| D2S303 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 2 | 2969.0 | | UniSTS | Human Whitehead-YAC Contig Map | 2 | | | UniSTS | Human Stanford-G3 RH Map | 2 | 3058.0 | | UniSTS | Human TNG Radiation Hybrid Map | 2 | 44799.0 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,199,435 - 70,199,574 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,199,409 - 70,199,633 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,462,602 - 70,462,818 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,462,628 - 70,462,759 | | UniSTS | Human Celera Assembly | 2 | 70,313,322 - 70,313,461 | | RGD | Human Celera Assembly | 2 | 70,313,296 - 70,313,520 | | UniSTS | Human Genome Assembly Build 36 | 2 | 70,316,132 - 70,316,263 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS | Genethon Human Genetic Map | 2 | 92.1 | | UniSTS | Marshfield Human Genetic Map | 2 | 88.15 | | RGD |
|
| D2S2113 |
| Map | Chr | Position | Strand | Source |
|---|
Human deCODE Assembly Map | 2 | 92.86 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,254,954 - 70,255,147 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,518,112 - 70,518,305 | | UniSTS | Human Celera Assembly | 2 | 70,368,803 - 70,368,996 | | RGD | Human Genome Assembly Build 36 | 2 | 70,371,616 - 70,371,809 | | RGD | Human Cytogenetic Map | 2 | p13.3 | | UniSTS | Human Cytogenetic Map | 2 | p13 | | UniSTS | Genethon Human Genetic Map | 2 | 92.3 | | UniSTS | Marshfield Human Genetic Map | 2 | 88.15 | | UniSTS | Marshfield Human Genetic Map | 2 | 88.15 | | RGD |
|
| WI-11889 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 2 | 291.4 | | UniSTS | Human GeneMap99-GB4 RH Map | 2 | 218.17 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,174,124 - 70,174,254 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,437,354 - 70,437,484 | | UniSTS | Human Celera Assembly | 2 | 70,288,048 - 70,288,178 | | RGD | Human Genome Assembly Build 36 | 2 | 70,290,858 - 70,290,988 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| RH81041 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 225.29 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,176,019 - 70,176,219 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,439,249 - 70,439,449 | | UniSTS | Human Celera Assembly | 2 | 70,289,943 - 70,290,143 | | RGD | Human Genome Assembly Build 36 | 2 | 70,292,753 - 70,292,953 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| D2S1873 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 70,192,607 - 70,192,729 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,455,837 - 70,455,959 | | UniSTS | Human Celera Assembly | 2 | 70,306,531 - 70,306,653 | | RGD | Human Genome Assembly Build 36 | 2 | 70,309,341 - 70,309,463 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| RH47301 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 224.15 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,175,362 - 70,175,493 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,438,592 - 70,438,723 | | UniSTS | Human Celera Assembly | 2 | 70,289,286 - 70,289,417 | | RGD | Human Genome Assembly Build 36 | 2 | 70,292,096 - 70,292,227 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| SHGC-32459 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 2 | 2976.0 | | UniSTS | Human Whitehead-RH Map | 2 | 298.9 | | UniSTS | Human Stanford-G3 RH Map | 2 | 3065.0 | | UniSTS | Human TNG Radiation Hybrid Map | 2 | 44759.0 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,173,377 - 70,173,509 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,436,607 - 70,436,739 | | UniSTS | Human Celera Assembly | 2 | 70,287,301 - 70,287,433 | | RGD | Human Genome Assembly Build 36 | 2 | 70,290,111 - 70,290,243 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| SHGC-58269 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 70,182,731 - 70,182,829 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,445,964 - 70,446,062 | | UniSTS | Human Celera Assembly | 2 | 70,296,655 - 70,296,753 | | RGD | Human Genome Assembly Build 36 | 2 | 70,299,468 - 70,299,566 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| SHGC-64100 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 2 | 44790.0 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,173,483 - 70,173,586 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,436,713 - 70,436,816 | | UniSTS | Human Celera Assembly | 2 | 70,287,407 - 70,287,510 | | RGD | Human Genome Assembly Build 36 | 2 | 70,290,217 - 70,290,320 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| WI-21718 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 2 | 385.8 | | UniSTS | Human Whitehead-RH Map | 2 | 284.9 | | UniSTS | Human GeneMap99-GB4 RH Map | 2 | 224.87 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,175,385 - 70,175,668 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,438,615 - 70,438,898 | | UniSTS | Human Celera Assembly | 2 | 70,289,309 - 70,289,592 | | RGD | Human Genome Assembly Build 36 | 2 | 70,292,119 - 70,292,402 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| RH68286 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 224.15 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,175,487 - 70,175,668 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,438,717 - 70,438,898 | | UniSTS | Human Celera Assembly | 2 | 70,289,411 - 70,289,592 | | RGD | Human Genome Assembly Build 36 | 2 | 70,292,221 - 70,292,402 | | RGD | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| RH48876 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 226.01 | | UniSTS | Human Genome Assembly HuRef | 2 | 70,180,312 - 70,180,884 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 70,443,542 - 70,444,114 | | UniSTS | Human Celera Assembly | 2 | 70,294,236 - 70,294,808 | | UniSTS | Human Cytogenetic Map | 2 | p13 | | UniSTS |
|
| D2S303 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 2 | | | UniSTS | Human Cytogenetic Map | 2 | p13 | | UniSTS | Genethon Human Genetic Map | 2 | 92.1 | | UniSTS | Marshfield Human Genetic Map | 2 | 88.15 | | UniSTS |
|