| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127858096-127858352 | Common:4; Rare:100 | ||||
| chr2:127885886-127885985 | Rare:26 | ||||
| chr2:127886209-127886504 | Common:1; Rare:77 | ||||
| chr2:128091004-128091354 | Common:8; Rare:122 | ||||
| chr2:130129330-130129621 | Common:4; Rare:78 | ||||
| chr2:130181546-130181744 | Common:2; Rare:89 | ||||
| chr2:130342102-130342242 | Rare:61; Clinvar:1 | ||||
| chr2:130342645-130342930 | Common:5; Rare:89 | ||||
| chr2:130372552-130372702 | Rare:45 | ||||
| chr2:131093359-131093559 | Common:1; Rare:92 | ||||
| chr2:131105193-131105367 | Common:1; Rare:79 | ||||
| chr2:131492310-131492445 | Common:3; Rare:58 | ||||
| chr2:131492749-131493086 | Common:8; Rare:101 | ||||
| chr2:134918597-134918863 | Common:1; Rare:106 | ||||
| chr2:135052212-135052323 | Common:1; Rare:48; Clinvar (benign):1 |