| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74508116-74508401 | Rare:57 | ||||
| chr2:74513169-74513701 | Rare:108 | ||||
| chr2:74514252-74514476 | Rare:49 | ||||
| chr2:74529607-74529980 | Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74530512-74530645 | Common:1; Rare:46; Clinvar:2 | ||||
| chr2:74553892-74554073 | Rare:26 | ||||
| chr2:74554406-74554755 | Common:2; Rare:102 | ||||
| chr2:74833842-74834153 | Rare:91 | ||||
| chr2:74835133-74835325 | Rare:49 | ||||
| chr2:74958560-74958697 | Common:2; Rare:51 | ||||
| chr2:74958877-74959032 | Rare:58 | ||||
| chr2:75647026-75647187 | Common:1; Rare:48 | ||||
| chr2:75710634-75710770 | Common:2; Rare:56 | ||||
| chr2:80304416-80304646 | Common:2; Rare:44 | ||||
| chr2:84459187-84459615 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |