| WI-19949 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 2 | 771.6 | | UniSTS | Human GeneMap99-GB4 RH Map | 2 | 477.31 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,706,423 - 127,706,622 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,714,730 - 135,714,929 | | UniSTS | Human Celera Assembly | 2 | 129,427,653 - 129,427,852 | | RGD | Human Genome Assembly Build 36 | 2 | 135,431,200 - 135,431,399 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|
| RH48571 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 477.59 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,704,122 - 127,704,275 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,712,428 - 135,712,581 | | UniSTS | Human Celera Assembly | 2 | 129,425,351 - 129,425,504 | | RGD | Human Genome Assembly Build 36 | 2 | 135,428,898 - 135,429,051 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|
| RH93392 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 472.72 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,700,684 - 127,700,813 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,708,990 - 135,709,119 | | UniSTS | Human Celera Assembly | 2 | 129,421,913 - 129,422,042 | | RGD | Human Genome Assembly Build 36 | 2 | 135,425,460 - 135,425,589 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|
| RH99330 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 472.72 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,708,143 - 127,708,294 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,716,450 - 135,716,601 | | UniSTS | Human Celera Assembly | 2 | 129,429,373 - 129,429,524 | | RGD | Human Genome Assembly Build 36 | 2 | 135,432,920 - 135,433,071 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|
| RH93172 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 472.78 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,707,216 - 127,707,344 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,715,523 - 135,715,651 | | UniSTS | Human Celera Assembly | 2 | 129,428,446 - 129,428,574 | | RGD | Human Genome Assembly Build 36 | 2 | 135,431,993 - 135,432,121 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|
| SHGC-143906 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 2 | 78742.0 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,670,192 - 127,670,472 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,678,498 - 135,678,778 | | UniSTS | Human Celera Assembly | 2 | 129,391,421 - 129,391,701 | | RGD | Human Genome Assembly Build 36 | 2 | 135,394,968 - 135,395,248 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|
| RH65103 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 2 | 1038.5 | | UniSTS | Human GeneMap99-GB4 RH Map | 2 | 480.23 | | UniSTS | Human Genome Assembly HuRef | 2 | 127,706,099 - 127,706,201 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 135,714,406 - 135,714,508 | | UniSTS | Human Celera Assembly | 2 | 129,427,329 - 129,427,431 | | RGD | Human Genome Assembly Build 36 | 2 | 135,430,876 - 135,430,978 | | RGD | Human Cytogenetic Map | 2 | q21.3 | | UniSTS |
|