| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98593467-98593801 | Common:2; Rare:104; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644581-98645305 | Common:7; Rare:220 | ||||
| chr12:100142816-100142989 | Common:1; Rare:71 | ||||
| chr12:100200717-100200876 | Rare:53 | ||||
| chr12:100266956-100267286 | Common:2; Rare:158 | ||||
| chr12:100573557-100573798 | Rare:80 | ||||
| chr12:101407654-101408100 | Common:3; Rare:120 | ||||
| chr12:101697581-101697680 | Common:2; Rare:26 | ||||
| chr12:101877531-101877797 | Common:5; Rare:67 | ||||
| chr12:102061948-102062184 | Common:1; Rare:67 | ||||
| chr12:102120043-102120470 | Common:3; Rare:133 | ||||
| chr12:103841256-103841454 | Common:3; Rare:66 | ||||
| chr12:103930022-103930594 | Common:9; Rare:188 | ||||
| chr12:103957109-103957335 | Common:6; Rare:65 | ||||
| chr12:103965661-103965986 | Common:2; Rare:78 |