| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112409554-112409707 | Common:1; Rare:52 | ||||
| chr12:112906838-112907029 | Rare:39 | ||||
| chr12:112938331-112938531 | Common:3; Rare:40 | ||||
| chr12:113135685-113135872 | Common:1; Rare:26 | ||||
| chr12:113185391-113185805 | Common:10; Rare:157 | ||||
| chr12:113221026-113221492 | Common:4; Rare:125 | ||||
| chr12:113359429-113359439 | Common:1 | ||||
| chr12:113421989-113422305 | Common:2; Rare:50 | ||||
| chr12:113422310-113422432 | Common:1; Rare:30 | ||||
| chr12:113966294-113966506 | Common:7; Rare:73 | ||||
| chr12:114682810-114682974 | Rare:39; Clinvar:3 | ||||
| chr12:114683200-114683456 | Common:3; Rare:61; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:114683560-114684534 | Common:8; Rare:232; Clinvar:6; Clinvar (benign):5 | ||||
| chr12:114684540-114684862 | Common:2; Rare:85 | ||||
| chr12:118016555-118016830 | Common:3; Rare:58 |