| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061297-118061612 | Common:6; Rare:50 | ||||
| chr12:118135986-118136237 | Common:2; Rare:69 | ||||
| chr12:118372772-118373189 | Common:2; Rare:111 | ||||
| chr12:120116629-120116935 | Common:5; Rare:87 | ||||
| chr12:120194683-120194790 | Rare:39 | ||||
| chr12:120201085-120201366 | Common:2; Rare:88 | ||||
| chr12:120438021-120438132 | Rare:38; Clinvar (benign):1 | ||||
| chr12:120446261-120446478 | Common:1; Rare:82 | ||||
| chr12:120469656-120469889 | Common:2; Rare:84 | ||||
| chr12:120495845-120496142 | Common:4; Rare:95 | ||||
| chr12:120687345-120687445 | Rare:33 | ||||
| chr12:121210097-121210146 | Rare:18 | ||||
| chr12:121352161-121352174 | Rare:2 | ||||
| chr12:121352351-121352629 | Common:3; Rare:94 | ||||
| chr12:121399902-121400177 | Common:5; Rare:103 |