| D4S1036 |
| Map | Chr | Position | Strand | Source |
|---|
Human Stanford-G3 RH Map | 4 | 3208.0 | | UniSTS | Human TNG Radiation Hybrid Map | 4 | 29045.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,804,814 - 49,804,965 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,860,711 - 53,860,862 | | UniSTS | Human Celera Assembly | 4 | 51,357,294 - 51,357,445 | | RGD | Human Genome Assembly Build 36 | 4 | 53,555,468 - 53,555,619 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| G41945 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 28868.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,750,648 - 49,750,899 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,806,572 - 53,806,823 | | UniSTS | Human Celera Assembly | 4 | 51,303,130 - 51,303,381 | | RGD | Human Genome Assembly Build 36 | 4 | 53,501,329 - 53,501,580 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-68272 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29021.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,814,211 - 49,814,431 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,870,108 - 53,870,328 | | UniSTS | Human Celera Assembly | 4 | 51,366,691 - 51,366,911 | | RGD | Human Genome Assembly Build 36 | 4 | 53,564,865 - 53,565,085 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-68563 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 28899.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,703,008 - 49,703,250 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,758,935 - 53,759,177 | | UniSTS | Human Celera Assembly | 4 | 51,255,489 - 51,255,731 | | RGD | Human Genome Assembly Build 36 | 4 | 53,453,692 - 53,453,934 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| RH122787 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29211.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,887,502 - 49,887,814 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,942,882 - 53,943,194 | | UniSTS | Human Celera Assembly | 4 | 51,439,512 - 51,439,824 | | RGD | Human Genome Assembly Build 36 | 4 | 53,637,639 - 53,637,951 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-110508 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29310.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 50,127,273 - 50,127,551 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,181,526 - 54,181,804 | | UniSTS | Human Celera Assembly | 4 | 51,679,008 - 51,679,286 | | RGD | Human Genome Assembly Build 36 | 4 | 53,876,283 - 53,876,561 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-111626 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29310.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 50,123,934 - 50,124,246 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,178,187 - 54,178,499 | | UniSTS | Human Celera Assembly | 4 | 51,675,669 - 51,675,981 | | RGD | Human Genome Assembly Build 36 | 4 | 53,872,944 - 53,873,256 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-148110 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29290.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 50,045,087 - 50,045,357 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,099,062 - 54,099,332 | | UniSTS | Human Celera Assembly | 4 | 51,595,701 - 51,595,971 | | RGD | Human Genome Assembly Build 36 | 4 | 53,793,819 - 53,794,089 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-153642 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29260.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,966,134 - 49,966,406 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,021,515 - 54,021,787 | | UniSTS | Human Celera Assembly | 4 | 51,518,158 - 51,518,430 | | RGD | Human Genome Assembly Build 36 | 4 | 53,716,272 - 53,716,544 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-100863 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29252.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,945,655 - 49,945,945 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,001,049 - 54,001,339 | | UniSTS | Human Celera Assembly | 4 | 51,497,664 - 51,497,954 | | RGD | Human Genome Assembly Build 36 | 4 | 53,695,806 - 53,696,096 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-112148 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29410.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 50,172,416 - 50,172,706 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,227,268 - 54,227,558 | | UniSTS | Human Celera Assembly | 4 | 51,724,753 - 51,725,043 | | RGD | Human Genome Assembly Build 36 | 4 | 53,922,025 - 53,922,315 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-155524 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 29319.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 50,100,903 - 50,101,008 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 54,155,154 - 54,155,259 | | UniSTS | Human Celera Assembly | 4 | 51,652,636 - 51,652,741 | | RGD | Human Genome Assembly Build 36 | 4 | 53,849,911 - 53,850,016 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| SHGC-56914 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 4 | 28907.0 | | UniSTS | Human Genome Assembly HuRef | 4 | 49,682,993 - 49,683,092 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,738,913 - 53,739,012 | | UniSTS | Human Celera Assembly | 4 | 51,235,466 - 51,235,565 | | RGD | Human Genome Assembly Build 36 | 4 | 53,433,670 - 53,433,769 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|
| D4S971 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 4 | 49,810,151 - 49,810,363 | | UniSTS | Human Genome Assembly GRCh37 | 4 | 53,866,048 - 53,866,260 | | UniSTS | Human Celera Assembly | 4 | 51,362,631 - 51,362,843 | | RGD | Human Genome Assembly Build 36 | 4 | 53,560,805 - 53,561,017 | | RGD | Human Cytogenetic Map | 4 | q12 | | UniSTS |
|