| RH65165 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 1 | 112,833,336 - 112,833,485 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 114,974,770 - 114,974,919 | | UniSTS | Human Celera Assembly | 1 | 113,203,998 - 113,204,147 | | RGD | Human Genome Assembly Build 36 | 1 | 114,776,293 - 114,776,442 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| SHGC-82151 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 1 | 62734.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 112,863,695 - 112,864,034 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 115,005,129 - 115,005,468 | | UniSTS | Human Celera Assembly | 1 | 113,234,355 - 113,234,694 | | RGD | Human Genome Assembly Build 36 | 1 | 114,806,652 - 114,806,991 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| G61971 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 1 | 112,861,144 - 112,861,427 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 115,002,582 - 115,002,865 | | UniSTS | Human Celera Assembly | 1 | 113,231,809 - 113,232,092 | | RGD | Human Genome Assembly Build 36 | 1 | 114,804,105 - 114,804,388 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| D1S2219 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly GRCh37 | 1 | 114,977,801 - 114,977,869 | | UniSTS | Human Celera Assembly | 1 | 113,207,029 - 113,207,097 | | RGD | Human Genome Assembly Build 36 | 1 | 114,779,324 - 114,779,392 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| WI-12516 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 1 | 427.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 1 | 371.65 | | UniSTS | Human Genome Assembly HuRef | 1 | 112,797,153 - 112,797,277 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 114,938,590 - 114,938,714 | | UniSTS | Human Celera Assembly | 1 | 113,167,820 - 113,167,944 | | RGD | Human Genome Assembly Build 36 | 1 | 114,740,113 - 114,740,237 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| AL009900 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 1 | 112,871,975 - 112,872,063 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 115,013,409 - 115,013,497 | | UniSTS | Human Celera Assembly | 1 | 113,242,635 - 113,242,723 | | RGD | Human Genome Assembly Build 36 | 1 | 114,814,932 - 114,815,020 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| SHGC-75347 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 1 | 799.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 1 | 370.7 | | UniSTS | Human TNG Radiation Hybrid Map | 1 | 62629.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 112,798,538 - 112,798,628 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 114,939,975 - 114,940,065 | | UniSTS | Human Celera Assembly | 1 | 113,169,205 - 113,169,295 | | RGD | Human Genome Assembly Build 36 | 1 | 114,741,498 - 114,741,588 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| SHGC-75367 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 1 | 374.12 | | UniSTS | Human TNG Radiation Hybrid Map | 1 | 62668.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 112,806,305 - 112,806,518 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 114,947,742 - 114,947,955 | | UniSTS | Human Celera Assembly | 1 | 113,176,971 - 113,177,184 | | RGD | Human Genome Assembly Build 36 | 1 | 114,749,265 - 114,749,478 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| SHGC-75362 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 1 | 372.38 | | UniSTS | Human TNG Radiation Hybrid Map | 1 | 62650.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 112,795,618 - 112,795,768 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 114,937,055 - 114,937,205 | | UniSTS | Human Celera Assembly | 1 | 113,166,285 - 113,166,435 | | RGD | Human Genome Assembly Build 36 | 1 | 114,738,578 - 114,738,728 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|
| SHGC-75356 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 1 | 790.3 | | UniSTS | Human GeneMap99-GB4 RH Map | 1 | 371.31 | | UniSTS | Human TNG Radiation Hybrid Map | 1 | 62654.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 112,797,188 - 112,797,323 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 114,938,625 - 114,938,760 | | UniSTS | Human Celera Assembly | 1 | 113,167,855 - 113,167,990 | | RGD | Human Genome Assembly Build 36 | 1 | 114,740,148 - 114,740,283 | | RGD | Human Cytogenetic Map | 1 | p13.1 | | UniSTS |
|