| D4S2994 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,503,258 - 21,503,406 | | UniSTS | Human Celera Assembly | 4 | 21,953,755 - 21,953,903 | | RGD | Human Genome Assembly Build 36 | 4 | 21,112,356 - 21,112,504 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.7 | | UniSTS | Marshfield Human Genetic Map | 4 | 36.09 | | UniSTS | Marshfield Human Genetic Map | 4 | 36.09 | | RGD |
|
| D4S1593 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1273.0 | | UniSTS | Human NCBI RH Map | 4 | 242.2 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Whitehead-RH Map | 4 | 99.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 85.83 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1289.0 | | UniSTS | Human deCODE Assembly Map | 4 | 36.76 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13457.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,588,178 - 20,588,371 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,588,049 - 20,588,200 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,244,575 - 21,244,768 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,244,444 - 21,244,597 | | UniSTS | Human Celera Assembly | 4 | 21,695,084 - 21,695,235 | | RGD | Human Celera Assembly | 4 | 21,695,213 - 21,695,406 | | UniSTS | Human Genome Assembly Build 36 | 4 | 20,853,542 - 20,853,695 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.2 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD |
|
| GATA70E01 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,461,863 - 20,462,026 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,113,572 - 21,113,735 | | UniSTS | Human Celera Assembly | 4 | 21,569,697 - 21,569,860 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD |
|
| D4S1533 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,215,354 - 21,215,541 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,871,306 - 21,871,497 | | UniSTS | Human Celera Assembly | 4 | 22,321,641 - 22,321,828 | | RGD | Human Genome Assembly Build 36 | 4 | 21,480,404 - 21,480,595 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD |
|
| D4S1546 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1243.0 | | UniSTS | Human NCBI RH Map | 4 | 235.9 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Stanford-G3 RH Map | 4 | 1259.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13239.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,115,118 - 20,115,268 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,115,015 - 20,115,166 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,766,376 - 20,766,526 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,766,277 - 20,766,424 | | UniSTS | Human Celera Assembly | 4 | 21,222,871 - 21,223,021 | | RGD | Human Celera Assembly | 4 | 21,222,766 - 21,222,919 | | UniSTS | Human Genome Assembly Build 36 | 4 | 20,375,474 - 20,375,624 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.2 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD |
|
| D4S3020 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13508.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,605,102 - 20,605,228 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,261,471 - 21,261,591 | | UniSTS | Human Celera Assembly | 4 | 21,712,112 - 21,712,235 | | RGD | Human Genome Assembly Build 36 | 4 | 20,870,569 - 20,870,689 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.2 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS |
|
| D4S1562 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1277.0 | | UniSTS | Human NCBI RH Map | 4 | 242.5 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Stanford-G3 RH Map | 4 | 1293.0 | | UniSTS | Human deCODE Assembly Map | 4 | 36.76 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13512.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,627,511 - 20,627,728 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,627,747 - 20,627,852 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,284,034 - 21,284,143 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,283,798 - 21,284,015 | | UniSTS | Human Celera Assembly | 4 | 21,734,440 - 21,734,657 | | UniSTS | Human Celera Assembly | 4 | 21,734,676 - 21,734,783 | | RGD | Human Genome Assembly Build 36 | 4 | 20,893,132 - 20,893,241 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.2 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD |
|
| D4S3017 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1296.0 | | UniSTS | Human NCBI RH Map | 4 | 243.3 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Stanford-G3 RH Map | 4 | 1312.0 | | UniSTS | Human deCODE Assembly Map | 4 | 37.16 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13646.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,812,540 - 20,812,735 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,468,657 - 21,468,848 | | UniSTS | Human Celera Assembly | 4 | 21,919,176 - 21,919,367 | | RGD | Human Genome Assembly Build 36 | 4 | 21,077,755 - 21,077,946 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.7 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.56 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.56 | | RGD |
|
| D4S2905 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Genome Assembly HuRef | 4 | 20,653,934 - 20,654,185 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,310,235 - 21,310,484 | | UniSTS | Human Celera Assembly | 4 | 21,760,856 - 21,761,105 | | RGD | Human Genome Assembly Build 36 | 4 | 20,919,333 - 20,919,582 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.2 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | RGD | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS |
|
| SHGC-51639 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13249.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,139,775 - 20,139,891 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,791,024 - 20,791,140 | | UniSTS | Human Celera Assembly | 4 | 21,247,518 - 21,247,634 | | RGD | Human Genome Assembly Build 36 | 4 | 20,400,122 - 20,400,238 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-8260 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13350.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,334,351 - 20,334,490 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,986,100 - 20,986,239 | | UniSTS | Human Celera Assembly | 4 | 21,442,247 - 21,442,386 | | RGD | Human Genome Assembly Build 36 | 4 | 20,595,198 - 20,595,337 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-24820 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1264.0 | | UniSTS | Human NCBI RH Map | 4 | 241.6 | | UniSTS | Human Whitehead-RH Map | 4 | 97.9 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 87.03 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1280.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,337,222 - 20,337,357 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,988,971 - 20,989,106 | | UniSTS | Human Celera Assembly | 4 | 21,445,118 - 21,445,253 | | RGD | Human Genome Assembly Build 36 | 4 | 20,598,069 - 20,598,204 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| STS-H52461 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 251.1 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 89.76 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,016,304 - 21,016,445 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,672,737 - 21,672,878 | | UniSTS | Human Celera Assembly | 4 | 22,123,178 - 22,123,319 | | RGD | Human Genome Assembly Build 36 | 4 | 21,281,835 - 21,281,976 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G16780 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,162,969 - 20,163,118 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,814,274 - 20,814,423 | | UniSTS | Human Celera Assembly | 4 | 21,270,765 - 21,270,914 | | RGD | Human Genome Assembly Build 36 | 4 | 20,423,372 - 20,423,521 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S3356 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,988,954 - 20,989,162 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,645,379 - 21,645,590 | | UniSTS | Human Celera Assembly | 4 | 22,095,822 - 22,096,033 | | RGD | Human Genome Assembly Build 36 | 4 | 21,254,477 - 21,254,688 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2792 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 247.4 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Whitehead-RH Map | 4 | 103.4 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 89.01 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13672.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13676.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,863,792 - 20,863,999 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,519,961 - 21,520,168 | | UniSTS | Human Celera Assembly | 4 | 21,970,455 - 21,970,662 | | RGD | Human Genome Assembly Build 36 | 4 | 21,129,059 - 21,129,266 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| STS-F04275 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 88.34 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,003,466 - 21,003,528 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,659,898 - 21,659,960 | | UniSTS | Human Celera Assembly | 4 | 22,110,339 - 22,110,401 | | RGD | Human Genome Assembly Build 36 | 4 | 21,268,996 - 21,269,058 | | RGD | Human Cytogenetic Map | 4 | p15.31 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-67709 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 241.6 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 85.83 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,678,306 - 20,678,467 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,334,595 - 21,334,756 | | UniSTS | Human Celera Assembly | 4 | 21,785,216 - 21,785,377 | | RGD | Human Genome Assembly Build 36 | 4 | 20,943,693 - 20,943,854 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2353 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Genome Assembly HuRef | 4 | 20,966,300 - 20,966,503 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,622,717 - 21,622,920 | | UniSTS | Human Celera Assembly | 4 | 22,073,166 - 22,073,369 | | RGD | Human Genome Assembly Build 36 | 4 | 21,231,815 - 21,232,018 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-67313 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 85.53 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13229.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,084,614 - 20,084,809 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,735,854 - 20,736,049 | | UniSTS | Human Celera Assembly | 4 | 21,192,359 - 21,192,554 | | RGD | Human Genome Assembly Build 36 | 4 | 20,344,952 - 20,345,147 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH17093 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,239,814 - 20,240,012 | | UniSTS | Human Genome Assembly HuRef | 1 | 113,105,642 - 113,105,840 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,891,130 - 20,891,328 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 115,247,168 - 115,247,366 | | UniSTS | Human Celera Assembly | 4 | 21,347,621 - 21,347,819 | | UniSTS | Human Celera Assembly | 1 | 113,476,425 - 113,476,623 | | RGD | Human Genome Assembly Build 36 | 1 | 115,048,691 - 115,048,889 | | RGD | Human Cytogenetic Map | 1 | p13.2 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH92764 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 88.65 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,103,023 - 20,103,165 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,754,280 - 20,754,422 | | UniSTS | Human Celera Assembly | 4 | 21,210,769 - 21,210,911 | | RGD | Human Genome Assembly Build 36 | 4 | 20,363,378 - 20,363,520 | | RGD | Human Cytogenetic Map | 4 | p15.31 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH93232 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 87.63 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,078,519 - 20,078,684 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,729,759 - 20,729,924 | | UniSTS | Human Celera Assembly | 4 | 21,186,264 - 21,186,429 | | RGD | Human Genome Assembly Build 36 | 4 | 20,338,857 - 20,339,022 | | RGD | Human Cytogenetic Map | 4 | p15.31 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-79761 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,088,925 - 21,089,217 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,745,550 - 21,745,842 | | UniSTS | Human Celera Assembly | 4 | 22,195,977 - 22,196,269 | | RGD | Human Genome Assembly Build 36 | 4 | 21,354,648 - 21,354,940 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-81007 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13587.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,724,104 - 20,724,398 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,380,280 - 21,380,574 | | UniSTS | Human Celera Assembly | 4 | 21,830,811 - 21,831,105 | | RGD | Human Genome Assembly Build 36 | 4 | 20,989,378 - 20,989,672 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH119995 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13609.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,773,075 - 20,773,349 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,429,196 - 21,429,470 | | UniSTS | Human Celera Assembly | 4 | 21,879,713 - 21,879,987 | | RGD | Human Genome Assembly Build 36 | 4 | 21,038,294 - 21,038,568 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH120910 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 100533.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,237,647 - 21,237,765 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,892,891 - 21,893,009 | | UniSTS | Human Celera Assembly | 4 | 22,343,517 - 22,343,635 | | RGD | Human Genome Assembly Build 36 | 4 | 21,501,989 - 21,502,107 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH122272 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13362.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13368.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,340,382 - 20,340,674 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,992,131 - 20,992,423 | | UniSTS | Human Celera Assembly | 4 | 21,448,279 - 21,448,571 | | RGD | Human Genome Assembly Build 36 | 4 | 20,601,229 - 20,601,521 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH118939 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13557.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,685,183 - 20,685,506 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,341,470 - 21,341,793 | | UniSTS | Human Celera Assembly | 4 | 21,792,093 - 21,792,416 | | RGD | Human Genome Assembly Build 36 | 4 | 20,950,568 - 20,950,891 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G63700 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13343.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,333,835 - 20,334,135 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,985,584 - 20,985,884 | | UniSTS | Human Celera Assembly | 4 | 21,441,731 - 21,442,031 | | RGD | Human Genome Assembly Build 36 | 4 | 20,594,682 - 20,594,982 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G63730 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,099,817 - 21,100,087 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,756,442 - 21,756,712 | | UniSTS | Human Celera Assembly | 4 | 22,206,868 - 22,207,138 | | RGD | Human Genome Assembly Build 36 | 4 | 21,365,540 - 21,365,810 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S337 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13500.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,648,474 - 20,648,700 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,629,989 - 20,630,194 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,286,280 - 21,286,489 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,304,765 - 21,304,991 | | UniSTS | Human Celera Assembly | 4 | 21,755,386 - 21,755,612 | | RGD | Human Celera Assembly | 4 | 21,736,920 - 21,737,129 | | UniSTS | Human Genome Assembly Build 36 | 4 | 20,913,863 - 20,914,089 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2312 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,461,806 - 20,462,090 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,113,515 - 21,113,799 | | UniSTS | Human Celera Assembly | 4 | 21,569,640 - 21,569,924 | | RGD | Human Genome Assembly Build 36 | 4 | 20,722,613 - 20,722,897 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-144186 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13422.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,529,258 - 20,529,532 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,185,709 - 21,185,983 | | UniSTS | Human Celera Assembly | 4 | 21,636,347 - 21,636,621 | | RGD | Human Genome Assembly Build 36 | 4 | 20,794,807 - 20,795,081 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-30526 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1315.0 | | UniSTS | Human Whitehead-RH Map | 4 | 104.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 89.01 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,003,453 - 21,003,567 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,659,885 - 21,659,999 | | UniSTS | Human Celera Assembly | 4 | 22,110,326 - 22,110,440 | | RGD | Human Genome Assembly Build 36 | 4 | 21,268,983 - 21,269,097 | | RGD | Human Cytogenetic Map | 4 | p15.31 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G20630 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,239,814 - 20,240,012 | | UniSTS | Human Genome Assembly HuRef | 1 | 113,105,642 - 113,105,840 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,891,130 - 20,891,328 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 115,247,168 - 115,247,366 | | UniSTS | Human Celera Assembly | 4 | 21,347,621 - 21,347,819 | | UniSTS | Human Celera Assembly | 1 | 113,476,425 - 113,476,623 | | RGD | Human Genome Assembly Build 36 | 1 | 115,048,691 - 115,048,889 | | RGD | Human Cytogenetic Map | 1 | p13.2 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-59718 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 88.34 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,821,138 - 20,821,238 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,477,267 - 21,477,367 | | UniSTS | Human Celera Assembly | 4 | 21,927,774 - 21,927,874 | | RGD | Human Genome Assembly Build 36 | 4 | 21,086,365 - 21,086,465 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S323 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,139,771 - 20,139,896 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,791,020 - 20,791,145 | | UniSTS | Human Celera Assembly | 4 | 21,247,514 - 21,247,639 | | RGD | Human Genome Assembly Build 36 | 4 | 20,400,118 - 20,400,243 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G65558 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,042,014 - 21,042,471 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,698,449 - 21,698,906 | | UniSTS | Human Celera Assembly | 4 | 22,148,886 - 22,149,343 | | RGD | Human Genome Assembly Build 36 | 4 | 21,307,547 - 21,308,004 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2511E |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1319.0 | | UniSTS | Human NCBI RH Map | 4 | 251.1 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 92.87 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1335.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,863,844 - 20,863,991 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,520,013 - 21,520,160 | | UniSTS | Human Celera Assembly | 4 | 21,970,507 - 21,970,654 | | RGD | Human Genome Assembly Build 36 | 4 | 21,129,111 - 21,129,258 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G33687 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,101,575 - 21,101,741 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,758,202 - 21,758,368 | | UniSTS | Human Celera Assembly | 4 | 22,208,628 - 22,208,794 | | RGD | Human Genome Assembly Build 36 | 4 | 21,367,300 - 21,367,466 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-59731 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 85.73 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,081,640 - 20,081,777 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,732,880 - 20,733,017 | | UniSTS | Human Celera Assembly | 4 | 21,189,385 - 21,189,522 | | RGD | Human Genome Assembly Build 36 | 4 | 20,341,978 - 20,342,115 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S893 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,933,242 - 20,933,456 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,589,653 - 21,589,867 | | UniSTS | Human Celera Assembly | 4 | 22,040,105 - 22,040,319 | | RGD | Human Genome Assembly Build 36 | 4 | 21,198,751 - 21,198,965 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| AB055381 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,591,313 - 20,591,444 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,247,710 - 21,247,841 | | UniSTS | Human Celera Assembly | 4 | 21,698,348 - 21,698,479 | | RGD | Human Genome Assembly Build 36 | 4 | 20,856,808 - 20,856,939 | | RGD |
|
| WI-18093 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 4 | 100.1 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 88.34 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,971,618 - 20,971,747 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,628,037 - 21,628,166 | | UniSTS | Human Celera Assembly | 4 | 22,078,486 - 22,078,615 | | RGD | Human Genome Assembly Build 36 | 4 | 21,237,135 - 21,237,264 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G33938 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,201,075 - 20,201,419 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,852,395 - 20,852,739 | | UniSTS | Human Celera Assembly | 4 | 21,308,888 - 21,309,232 | | RGD | Human Genome Assembly Build 36 | 4 | 20,461,493 - 20,461,837 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| CHLC.GGAT14F06 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,714,386 - 20,714,505 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,370,541 - 21,370,660 | | UniSTS | Human Celera Assembly | 4 | 21,821,064 - 21,821,183 | | RGD | Human Genome Assembly Build 36 | 4 | 20,979,639 - 20,979,758 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-59487 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 241.6 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 87.93 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,329,656 - 20,329,801 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,981,405 - 20,981,550 | | UniSTS | Human Celera Assembly | 4 | 21,437,552 - 21,437,697 | | RGD | Human Genome Assembly Build 36 | 4 | 20,590,503 - 20,590,648 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2803 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,121,340 - 21,121,624 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,777,976 - 21,778,260 | | UniSTS | Human Celera Assembly | 4 | 22,228,300 - 22,228,584 | | RGD | Human Genome Assembly Build 36 | 4 | 21,387,074 - 21,387,358 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| RH12353 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 250.3 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 93.28 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,262,402 - 21,262,522 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,917,657 - 21,917,777 | | UniSTS | Human Celera Assembly | 4 | 22,368,288 - 22,368,408 | | RGD | Human Genome Assembly Build 36 | 4 | 21,526,755 - 21,526,875 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-50646 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13380.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,375,835 - 20,376,021 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,027,584 - 21,027,770 | | UniSTS | Human Genome Assembly Build 36 | 4 | 20,636,682 - 20,636,868 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-50148 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13462.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,588,009 - 20,588,367 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,244,404 - 21,244,764 | | UniSTS | Human Celera Assembly | 4 | 21,695,044 - 21,695,402 | | RGD | Human Genome Assembly Build 36 | 4 | 20,853,502 - 20,853,862 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| G33915 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 20,162,944 - 20,163,133 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,814,249 - 20,814,438 | | UniSTS | Human Celera Assembly | 4 | 21,270,740 - 21,270,929 | | RGD | Human Genome Assembly Build 36 | 4 | 20,423,347 - 20,423,536 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2708 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 100555.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,263,231 - 21,263,326 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,918,486 - 21,918,581 | | UniSTS | Human Celera Assembly | 4 | 22,369,117 - 22,369,212 | | RGD | Human Genome Assembly Build 36 | 4 | 21,527,584 - 21,527,679 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S278 |
| Map | Chr | Position | Strand | Source |
|---|
Human Stanford-G3 RH Map | 4 | 1331.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13781.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,017,484 - 21,017,642 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,673,917 - 21,674,075 | | UniSTS | Human Celera Assembly | 4 | 22,124,358 - 22,124,516 | | RGD | Human Genome Assembly Build 36 | 4 | 21,283,015 - 21,283,173 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| WI-20656 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 4 | 101.4 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 88.34 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,914,256 - 20,914,462 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,570,650 - 21,570,856 | | UniSTS | Human Celera Assembly | 4 | 22,021,103 - 22,021,309 | | RGD | Human Genome Assembly Build 36 | 4 | 21,179,748 - 21,179,954 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S503 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13520.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,628,351 - 20,628,500 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,284,642 - 21,284,791 | | UniSTS | Human Celera Assembly | 4 | 21,735,282 - 21,735,431 | | RGD | Human Genome Assembly Build 36 | 4 | 20,893,740 - 20,893,889 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-17216 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1311.0 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1327.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13705.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,914,235 - 20,914,378 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,570,629 - 21,570,772 | | UniSTS | Human Celera Assembly | 4 | 22,021,082 - 22,021,225 | | RGD | Human Genome Assembly Build 36 | 4 | 21,179,727 - 21,179,870 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S456 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Whitehead-RH Map | 4 | 104.1 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1276.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,263,593 - 20,263,790 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 20,914,897 - 20,915,094 | | UniSTS | Human Celera Assembly | 4 | 21,371,399 - 21,371,596 | | RGD | Human Genome Assembly Build 36 | 4 | 20,523,995 - 20,524,192 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-24104 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 100490.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,121,465 - 21,121,588 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,778,101 - 21,778,224 | | UniSTS | Human Celera Assembly | 4 | 22,228,425 - 22,228,548 | | RGD | Human Genome Assembly Build 36 | 4 | 21,387,199 - 21,387,322 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-51650 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13492.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,630,200 - 20,630,306 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,286,495 - 21,286,601 | | UniSTS | Human Celera Assembly | 4 | 21,737,135 - 21,737,241 | | RGD | Human Genome Assembly Build 36 | 4 | 20,895,593 - 20,895,699 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| WI-21155 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 247.4 | | UniSTS | Human Whitehead-RH Map | 4 | 103.6 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 89.01 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,819,556 - 20,819,633 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,475,687 - 21,475,764 | | UniSTS | Human Celera Assembly | 4 | 21,926,194 - 21,926,271 | | RGD | Human Genome Assembly Build 36 | 4 | 21,084,785 - 21,084,862 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2525E |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1323.0 | | UniSTS | Human NCBI RH Map | 4 | 244.5 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1339.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,121,439 - 21,121,513 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,778,075 - 21,778,149 | | UniSTS | Human Celera Assembly | 4 | 22,228,399 - 22,228,473 | | RGD | Human Genome Assembly Build 36 | 4 | 21,387,173 - 21,387,247 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S3349 |
| Map | Chr | Position | Strand | Source |
|---|
Human deCODE Assembly Map | 4 | 37.29 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,215,376 - 21,215,518 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,871,328 - 21,871,474 | | UniSTS | Human Celera Assembly | 4 | 22,321,663 - 22,321,805 | | RGD | Human Genome Assembly Build 36 | 4 | 21,480,426 - 21,480,572 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS |
|
| D4S2620 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human deCODE Assembly Map | 4 | 36.53 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13404.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 20,461,845 - 20,462,110 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,113,554 - 21,113,819 | | UniSTS | Human Celera Assembly | 4 | 21,569,679 - 21,569,944 | | RGD | Human Genome Assembly Build 36 | 4 | 20,722,652 - 20,722,917 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| SHGC-67835 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 88.34 | | UniSTS | Human Genome Assembly HuRef | 4 | 21,259,845 - 21,259,993 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,915,099 - 21,915,247 | | UniSTS | Human Celera Assembly | 4 | 22,365,731 - 22,365,879 | | RGD | Human Genome Assembly Build 36 | 4 | 21,524,197 - 21,524,345 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S2707 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 21,101,598 - 21,101,767 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 21,758,225 - 21,758,394 | | UniSTS | Human Celera Assembly | 4 | 22,208,651 - 22,208,820 | | RGD | Human Genome Assembly Build 36 | 4 | 21,367,323 - 21,367,492 | | RGD | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S1546 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1243.0 | | UniSTS | Human NCBI RH Map | 4 | 235.9 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1259.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13239.0 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S1562 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 1277.0 | | UniSTS | Human NCBI RH Map | 4 | 242.5 | | UniSTS | Human Stanford-G3 RH Map | 4 | 1293.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 13512.0 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|
| D4S1593 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 241.6 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Whitehead-RH Map | 4 | 99.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 85.83 | | UniSTS | Human deCODE Assembly Map | 4 | 36.76 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS | Genethon Human Genetic Map | 4 | 34.2 | | UniSTS | Marshfield Human Genetic Map | 4 | 35.03 | | UniSTS |
|
| D4S337 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 13500.0 | | UniSTS | Human Cytogenetic Map | 4 | p15.32 | | UniSTS |
|