| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:109632529-109632532 | Rare:1 | ||||
| chr2:112824303-112824454 | Rare:22 | ||||
| chr2:113324928-113325099 | Common:1; Rare:30 | ||||
| chr2:131055399-131055620 | Rare:72 | ||||
| chr2:131682362-131682504 | Common:2; Rare:40 | ||||
| chr2:134862713-134863032 | Rare:55 | ||||
| chr2:158132018-158132283 | Rare:40 | ||||
| chr2:159773166-159773290 | Common:1; Rare:25 | ||||
| chr2:160270394-160270623 | Common:1; Rare:49 | ||||
| chr2:161244645-161244841 | Common:1; Rare:58 | ||||
| chr2:162317901-162318058 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:162380148-162380233 | Rare:17 | ||||
| chr2:164622364-164622641 | Common:3; Rare:50 | ||||
| chr2:170770722-170771132 | Common:3; Rare:76 | ||||
| chr2:172487045-172487388 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):1 |