| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110306955-110307558 | Common:7; Rare:181; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110561668-110561889 | Common:5; Rare:79 | ||||
| chr13:110615329-110615647 | Common:3; Rare:105 | ||||
| chr13:110713018-110713266 | Common:2; Rare:108 | ||||
| chr13:111202780-111203093 | Common:1; Rare:43 | ||||
| chr13:113187285-113187602 | Common:2; Rare:57 | ||||
| chr13:113208614-113208756 | Rare:85 | ||||
| chr13:113490699-113490981 | Common:1; Rare:106 | ||||
| chr13:114281505-114281654 | Common:2; Rare:81 | ||||
| chr14:20343219-20343652 | Common:12; Rare:244 | ||||
| chr14:20413409-20413551 | Common:3; Rare:44 | ||||
| chr14:20454704-20455594 | Common:7; Rare:230 | ||||
| chr14:20684427-20684595 | Common:2; Rare:25; Clinvar (benign):2 | ||||
| chr14:21383881-21384252 | Common:8; Rare:118 | ||||
| chr14:21456041-21456348 | Common:4; Rare:78 |