| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100142859-100143013 | Common:2; Rare:55 | ||||
| chr12:100199977-100200088 | Rare:25 | ||||
| chr12:101407731-101408074 | Common:2; Rare:86 | ||||
| chr12:101877408-101877461 | Rare:11 | ||||
| chr12:101877510-101877720 | Common:3; Rare:57 | ||||
| chr12:102120058-102120256 | Rare:78 | ||||
| chr12:103930122-103930480 | Common:7; Rare:122 | ||||
| chr12:103965705-103965927 | Common:2; Rare:53 | ||||
| chr12:106301873-106301946 | Rare:19 | ||||
| chr12:106302762-106302882 | Common:4; Rare:40 | ||||
| chr12:106955526-106955917 | Rare:143 | ||||
| chr12:107685643-107685900 | Common:2; Rare:85 | ||||
| chr12:108562411-108562733 | Common:9; Rare:134; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633826-108634049 | Rare:50 | ||||
| chr12:109052527-109052600 | Common:1; Rare:19 |