| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123972553-123972895 | Common:6; Rare:118 | ||||
| chr12:123972994-123973314 | Common:2; Rare:104 | ||||
| chr12:124786667-124786793 | Rare:31 | ||||
| chr12:124914585-124914993 | Common:8; Rare:159 | ||||
| chr12:130953781-130954026 | Rare:51 | ||||
| chr12:131929018-131929280 | Common:10; Rare:80; Clinvar:1 | ||||
| chr12:132687322-132687744 | Common:4; Rare:152; Clinvar:2; Clinvar (benign):8 | ||||
| chr12:132710758-132711031 | Common:3; Rare:86 | ||||
| chr12:132829052-132829228 | Rare:84 | ||||
| chr12:132887548-132887781 | Rare:74 | ||||
| chr12:132956252-132956426 | Common:1; Rare:38 | ||||
| chr12:132986266-132986423 | Rare:35 | ||||
| chr12:133130238-133130627 | Common:7; Rare:121 | ||||
| chr13:19863623-19863972 | Common:4; Rare:133 | ||||
| chr13:20525793-20525942 | Common:1; Rare:62 |