| D4S2887 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 4 | 887.8 | | UniSTS | Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Whitehead-RH Map | 4 | 485.6 | | UniSTS | Human Stanford-G3 RH Map | 4 | 4207.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 43671.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,696,694 - 71,696,853 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,949,694 - 75,949,853 | | UniSTS | Human Celera Assembly | 4 | 73,244,990 - 73,245,149 | | RGD | Human Genome Assembly Build 36 | 4 | 76,168,718 - 76,168,877 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| A005X37 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 431.46 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,722,191 - 71,722,290 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,975,191 - 75,975,290 | | UniSTS | Human Celera Assembly | 4 | 73,270,487 - 73,270,586 | | RGD | Human Genome Assembly Build 36 | 4 | 76,194,215 - 76,194,314 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| G20578 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 71,722,191 - 71,722,290 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,975,191 - 75,975,290 | | UniSTS | Human Celera Assembly | 4 | 73,270,487 - 73,270,586 | | RGD | Human Genome Assembly Build 36 | 4 | 76,194,215 - 76,194,314 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| SHGC-36704 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 4 | 4182.0 | | UniSTS | Human NCBI RH Map | 4 | 889.2 | | UniSTS | Human Stanford-G3 RH Map | 4 | 4198.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 43696.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,722,174 - 71,722,259 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,975,174 - 75,975,259 | | UniSTS | Human Celera Assembly | 4 | 73,270,470 - 73,270,555 | | RGD | Human Genome Assembly Build 36 | 4 | 76,194,198 - 76,194,283 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| G20397 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 71,720,631 - 71,720,872 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,973,631 - 75,973,872 | | UniSTS | Human Celera Assembly | 4 | 73,268,927 - 73,269,168 | | RGD | Human Genome Assembly Build 36 | 4 | 76,192,655 - 76,192,896 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| A005P21 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 431.46 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,720,631 - 71,720,872 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,973,631 - 75,973,872 | | UniSTS | Human Celera Assembly | 4 | 73,268,927 - 73,269,168 | | RGD | Human Genome Assembly Build 36 | 4 | 76,192,655 - 76,192,896 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| WI-22409 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 4 | 485.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 4 | 437.45 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,719,433 - 71,719,647 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,972,433 - 75,972,647 | | UniSTS | Human Celera Assembly | 4 | 73,267,729 - 73,267,943 | | RGD | Human Genome Assembly Build 36 | 4 | 76,191,457 - 76,191,671 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| RH99328 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 4 | 428.12 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,666,236 - 71,666,390 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,919,235 - 75,919,389 | | UniSTS | Human Celera Assembly | 4 | 73,214,496 - 73,214,650 | | RGD | Human Genome Assembly Build 36 | 4 | 76,138,259 - 76,138,413 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| RH119553 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 43647.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,660,024 - 71,660,248 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,913,023 - 75,913,247 | | UniSTS | Human Celera Assembly | 4 | 73,208,284 - 73,208,508 | | RGD | Human Genome Assembly Build 36 | 4 | 76,132,047 - 76,132,271 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| RH119874 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 43652.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,702,932 - 71,703,265 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,955,932 - 75,956,265 | | UniSTS | Human Celera Assembly | 4 | 73,251,228 - 73,251,561 | | RGD | Human Genome Assembly Build 36 | 4 | 76,174,956 - 76,175,289 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| D4S2591E |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 71,720,648 - 71,720,804 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,973,648 - 75,973,804 | | UniSTS | Human Celera Assembly | 4 | 73,268,944 - 73,269,100 | | RGD | Human Genome Assembly Build 36 | 4 | 76,192,672 - 76,192,828 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| NIB1435 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 4 | | | UniSTS | Human Genome Assembly HuRef | 4 | 71,722,087 - 71,722,237 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,975,087 - 75,975,237 | | UniSTS | Human Celera Assembly | 4 | 73,270,383 - 73,270,533 | | RGD | Human Genome Assembly Build 36 | 4 | 76,194,111 - 76,194,261 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|
| D4S773 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 43628.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 71,615,246 - 71,615,401 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 75,868,245 - 75,868,400 | | UniSTS | Human Celera Assembly | 4 | 73,163,505 - 73,163,660 | | RGD | Human Genome Assembly Build 36 | 4 | 76,087,269 - 76,087,424 | | RGD | Human Cytogenetic Map | 4 | q13.3-q21.3 | | UniSTS |
|