| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980571-122980963 | Common:2; Rare:112 | ||||
| chr12:123105457-123105661 | Common:1; Rare:37 | ||||
| chr12:123233093-123233524 | Common:2; Rare:148; Clinvar:1 | ||||
| chr12:123364758-123364989 | Common:5; Rare:100 | ||||
| chr12:123584328-123584729 | Common:7; Rare:134 | ||||
| chr12:123602018-123602184 | Common:3; Rare:59 | ||||
| chr12:123633597-123633856 | Common:1; Rare:126; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972565-123972650 | Common:3; Rare:27 | ||||
| chr12:123973003-123973314 | Common:2; Rare:103 | ||||
| chr12:124388791-124388974 | Common:3; Rare:55 | ||||
| chr12:124389280-124389444 | Rare:36 | ||||
| chr12:124423020-124423340 | Common:2; Rare:78 | ||||
| chr12:124518258-124518383 | Common:2; Rare:31 | ||||
| chr12:124518527-124518744 | Rare:56 | ||||
| chr12:124786354-124786786 | Common:3; Rare:117 |