| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127858086-127858224 | Common:2; Rare:76 | ||||
| chr2:128091055-128091347 | Common:8; Rare:98 | ||||
| chr2:130129330-130129622 | Common:4; Rare:79 | ||||
| chr2:130181546-130181704 | Common:1; Rare:57 | ||||
| chr2:130342121-130342242 | Rare:50; Clinvar:1 | ||||
| chr2:130342645-130342927 | Common:5; Rare:88 | ||||
| chr2:130836781-130836936 | Common:2; Rare:68 | ||||
| chr2:131105194-131105351 | Common:1; Rare:66 | ||||
| chr2:131493041-131493097 | Common:1; Rare:14 | ||||
| chr2:134918567-134918859 | Common:1; Rare:114 | ||||
| chr2:135052167-135052306 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr2:135530710-135530970 | Common:3; Rare:61 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135876400-135876657 | Rare:66 | ||||
| chr2:135985407-135985685 | Common:4; Rare:123; Clinvar (benign):1 |