| GDB:595848 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 22 | 11,212,155 - 11,212,267 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,247,835 - 28,247,947 | | UniSTS | Human Genome Assembly GRCh37 | Un | 30,724 - 30,836 | | UniSTS | Human Celera Assembly | 22 | 12,047,800 - 12,047,912 | | RGD | Human Genome Assembly Build 36 | 22 | 26,577,835 - 26,577,947 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|
| D22S989E |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 22 | 77.86 | | UniSTS | Human Genome Assembly HuRef | 22 | 11,212,073 - 11,212,191 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,247,753 - 28,247,871 | | UniSTS | Human Genome Assembly GRCh37 | Un | 30,642 - 30,760 | | UniSTS | Human Celera Assembly | 22 | 12,047,718 - 12,047,836 | | RGD | Human Genome Assembly Build 36 | 22 | 26,577,753 - 26,577,871 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|
| SHGC-144047 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 22 | 5093.0 | | UniSTS | Human Genome Assembly HuRef | 22 | 11,225,897 - 11,226,236 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,261,574 - 28,261,913 | | UniSTS | Human Celera Assembly | 22 | 12,061,539 - 12,061,878 | | RGD | Human Genome Assembly Build 36 | 22 | 26,591,574 - 26,591,913 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|
| A006Q06 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 22 | 71.35 | | UniSTS | Human Genome Assembly HuRef | 22 | 11,213,391 - 11,213,581 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,249,071 - 28,249,261 | | UniSTS | Human Genome Assembly GRCh37 | Un | 31,960 - 32,150 | | UniSTS | Human Celera Assembly | 22 | 12,049,036 - 12,049,226 | | RGD | Human Genome Assembly Build 36 | 22 | 26,579,071 - 26,579,261 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|
| WI-11820 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 22 | 68.1 | | UniSTS | Human GeneMap99-GB4 RH Map | 22 | 71.87 | | UniSTS | Human Genome Assembly HuRef | 22 | 11,214,259 - 11,214,408 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,249,938 - 28,250,087 | | UniSTS | Human Genome Assembly GRCh37 | Un | 32,827 - 32,976 | | UniSTS | Human Celera Assembly | 22 | 12,049,903 - 12,050,052 | | RGD | Human Genome Assembly Build 36 | 22 | 26,579,938 - 26,580,087 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|
| D22S1104 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-YAC Contig Map | 22 | | | UniSTS | Human Genome Assembly HuRef | 22 | 11,211,979 - 11,212,184 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,247,659 - 28,247,864 | | UniSTS | Human Genome Assembly GRCh37 | Un | 30,548 - 30,753 | | UniSTS | Human Celera Assembly | 22 | 12,047,624 - 12,047,829 | | RGD | Human Genome Assembly Build 36 | 22 | 26,577,659 - 26,577,864 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|
| SGC31665 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 22 | 67.5 | | UniSTS | Human GeneMap99-GB4 RH Map | 22 | 73.2 | | UniSTS | Human Genome Assembly HuRef | 22 | 11,213,749 - 11,213,967 | | UniSTS | Human Genome Assembly GRCh37 | 22 | 28,249,429 - 28,249,647 | | UniSTS | Human Genome Assembly GRCh37 | Un | 32,318 - 32,536 | | UniSTS | Human Celera Assembly | 22 | 12,049,394 - 12,049,612 | | RGD | Human Genome Assembly Build 36 | 22 | 26,579,429 - 26,579,647 | | RGD | Human Cytogenetic Map | 22 | q12.1 | | UniSTS |
|