| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100142782-100142989 | Common:1; Rare:84 | ||||
| chr12:100200688-100200857 | Common:1; Rare:56 | ||||
| chr12:100266782-100266875 | Rare:24 | ||||
| chr12:100266969-100267316 | Common:2; Rare:159 | ||||
| chr12:100573549-100573700 | Rare:47 | ||||
| chr12:101407429-101407451 | Rare:6 | ||||
| chr12:101407459-101407549 | Rare:22 | ||||
| chr12:101407669-101408233 | Common:3; Rare:141 | ||||
| chr12:101664353-101664462 | Rare:31 | ||||
| chr12:101665943-101666156 | Common:3; Rare:27 | ||||
| chr12:101697504-101697992 | Common:5; Rare:158 | ||||
| chr12:101739344-101739625 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:101877480-101877739 | Common:3; Rare:67 | ||||
| chr12:102061954-102062197 | Rare:67 | ||||
| chr12:102120033-102120269 | Common:1; Rare:97 |