| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121626712-121626821 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:121627228-121627263 | Rare:5 | ||||
| chr12:121627295-121627443 | Rare:27 | ||||
| chr12:121672373-121672709 | Common:6; Rare:83 | ||||
| chr12:121712613-121712858 | Common:5; Rare:97 | ||||
| chr12:121793933-121794093 | Common:2; Rare:41 | ||||
| chr12:121800084-121800312 | Common:2; Rare:71 | ||||
| chr12:121800550-121800751 | Common:1; Rare:58 | ||||
| chr12:121800860-121801532 | Common:6; Rare:183 | ||||
| chr12:121802893-121803200 | Common:1; Rare:78 | ||||
| chr12:121803252-121803705 | Common:1; Rare:122 | ||||
| chr12:121804071-121804416 | Rare:121 | ||||
| chr12:121888397-121888920 | Common:3; Rare:147 | ||||
| chr12:121889018-121889199 | Rare:37 | ||||
| chr12:121915814-121916103 | Common:1; Rare:83 |