| SHGC-63465 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 17,612,236 - 17,612,346 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,837,134 - 17,837,244 | | UniSTS | Human Celera Assembly | 2 | 17,716,944 - 17,717,054 | | RGD | Human Genome Assembly Build 36 | 2 | 17,700,615 - 17,700,725 | | RGD | Human Cytogenetic Map | 2 | p24.3 | | UniSTS |
|
| RH80046 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 17,612,345 - 17,612,533 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,837,243 - 17,837,431 | | UniSTS | Human Celera Assembly | 2 | 17,717,053 - 17,717,241 | | RGD | Human Genome Assembly Build 36 | 2 | 17,700,724 - 17,700,912 | | RGD | Human Cytogenetic Map | 2 | p24.3 | | UniSTS |
|
| D2S1629E |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 17,612,337 - 17,612,532 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,837,235 - 17,837,430 | | UniSTS | Human Celera Assembly | 2 | 17,717,045 - 17,717,240 | | RGD | Human Genome Assembly Build 36 | 2 | 17,700,716 - 17,700,911 | | RGD | Human Cytogenetic Map | 2 | p24.3 | | UniSTS |
|
| SHGC-133056 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 2 | 14477.0 | | UniSTS | Human Genome Assembly HuRef | 2 | 17,612,239 - 17,612,346 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,837,137 - 17,837,244 | | UniSTS | Human Celera Assembly | 2 | 17,716,947 - 17,717,054 | | RGD | Human Genome Assembly Build 36 | 2 | 17,700,618 - 17,700,725 | | RGD | Human Cytogenetic Map | 2 | p24.3 | | UniSTS |
|
| BMON121 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 17,611,783 - 17,611,947 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,836,671 - 17,836,845 | | UniSTS | Human Celera Assembly | 2 | 17,716,481 - 17,716,655 | | RGD | Human Genome Assembly Build 36 | 2 | 17,700,152 - 17,700,326 | | RGD |
|
| D2S1414 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 2 | | | UniSTS | Human Genome Assembly HuRef | 2 | 17,552,133 - 17,552,387 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,777,058 - 17,777,312 | | UniSTS | Human Celera Assembly | 2 | 17,656,869 - 17,657,123 | | RGD | Human Genome Assembly Build 36 | 2 | 17,640,539 - 17,640,793 | | RGD | Human Cytogenetic Map | 2 | p24.3 | | UniSTS |
|
| D6Arb7 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 17,611,711 - 17,611,915 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,836,599 - 17,836,813 | | UniSTS | Human Celera Assembly | 2 | 17,716,409 - 17,716,623 | | UniSTS |
|
| D6Rat38 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 17,611,811 - 17,611,947 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 17,836,699 - 17,836,845 | | UniSTS | Human Celera Assembly | 2 | 17,716,509 - 17,716,655 | | UniSTS |
|
| AU048745 |
| Map | Chr | Position | Strand | Source |
|---|
Human Cytogenetic Map | 22 | q13.1 | | UniSTS | Human Cytogenetic Map | 7 | q34 | | UniSTS | Human Cytogenetic Map | 12 | q24.23 | | UniSTS | Human Cytogenetic Map | 19 | p13.2 | | UniSTS | Human Cytogenetic Map | 2 | p24.3 | | UniSTS | Human Cytogenetic Map | 19 | q13.2 | | UniSTS | Human Cytogenetic Map | 14 | q31.3 | | UniSTS | Human Cytogenetic Map | 3 | p23-p21 | | UniSTS | Human Cytogenetic Map | 6 | p21.1 | | UniSTS | Human Cytogenetic Map | 12 | q24.32 | | UniSTS | Human Cytogenetic Map | 11 | p11.2 | | UniSTS | Human Cytogenetic Map | 1 | q21.2 | | UniSTS | Human Cytogenetic Map | 21 | q22.1 | | UniSTS | Human Cytogenetic Map | 6 | q16.1 | | UniSTS | Human Cytogenetic Map | 2 | q14.2-q14.3 | | UniSTS | Human Cytogenetic Map | 1 | p34.3 | | UniSTS | Human Cytogenetic Map | 6 | p22.1 | | UniSTS | Human Cytogenetic Map | 22 | q13.2 | | UniSTS | Human Cytogenetic Map | 7 | q21.12 | | UniSTS | Human Cytogenetic Map | 19 | p13.11 | | UniSTS | Human Cytogenetic Map | 15 | q24-q25 | | UniSTS | Human Cytogenetic Map | X | q23 | | UniSTS |
|