| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131034866-131035176 | Common:1; Rare:83 | ||||
| chr2:131093341-131093571 | Common:1; Rare:100 | ||||
| chr2:131105193-131105375 | Common:1; Rare:84 | ||||
| chr2:131492059-131492217 | Common:3; Rare:48 | ||||
| chr2:131492310-131492558 | Common:8; Rare:104 | ||||
| chr2:131492749-131493107 | Common:8; Rare:110 | ||||
| chr2:132257728-132257882 | Common:1; Rare:33 | ||||
| chr2:132257899-132258033 | Common:5; Rare:29 | ||||
| chr2:134918580-134918908 | Common:1; Rare:136 | ||||
| chr2:135052198-135052310 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135586212-135586490 | Rare:51 | ||||
| chr2:135985401-135985670 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr2:136118142-136118279 | Rare:39 | ||||
| chr2:138501661-138502020 | Common:2; Rare:129 |