| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124269-183124466 | Common:2; Rare:70 | ||||
| chr2:186485983-186486455 | Common:3; Rare:136 | ||||
| chr2:186589894-186590005 | Rare:32 | ||||
| chr2:186590255-186590372 | Rare:41 | ||||
| chr2:188291777-188292074 | Common:3; Rare:94 | ||||
| chr2:188292692-188292870 | Common:1; Rare:44 | ||||
| chr2:189179588-189179844 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:189441065-189441523 | Common:2; Rare:150 | ||||
| chr2:189580759-189580891 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189674510-189674580 | Rare:19 | ||||
| chr2:189783921-189784096 | Common:4; Rare:55; Clinvar (benign):1 | ||||
| chr2:189784262-189784551 | Common:4; Rare:104; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190062184-190062273 | Rare:32; Clinvar (pathogenic):1 | ||||
| chr2:190062325-190062522 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:190062689-190062832 | Rare:21 |