| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342642-130342923 | Common:4; Rare:86 | ||||
| chr2:130355827-130356102 | Common:3; Rare:79 | ||||
| chr2:131493034-131493097 | Common:1; Rare:16 | ||||
| chr2:134918588-134918876 | Common:1; Rare:120 | ||||
| chr2:135531172-135531502 | Common:1; Rare:66 | ||||
| chr2:135985429-135985670 | Common:4; Rare:110; Clinvar (benign):1 | ||||
| chr2:137964139-137964614 | Common:2; Rare:89 | ||||
| chr2:138501664-138502010 | Common:2; Rare:122 | ||||
| chr2:144517324-144517610 | Rare:80; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144520136-144520529 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr2:144524462-144524627 | Common:4; Rare:42 | ||||
| chr2:148020681-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021552-148021675 | Rare:23 | ||||
| chr2:148644474-148644751 | Rare:82 | ||||
| chr2:149587326-149587351 | Rare:6 |