| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120446245-120446471 | Common:1; Rare:81 | ||||
| chr12:120495915-120496139 | Common:3; Rare:61 | ||||
| chr12:120686947-120687184 | Common:1; Rare:82 | ||||
| chr12:121296682-121296932 | Common:1; Rare:77 | ||||
| chr12:122266392-122266547 | Common:2; Rare:66 | ||||
| chr12:122278907-122279054 | Common:1; Rare:42 | ||||
| chr12:122500838-122501171 | Common:3; Rare:89 | ||||
| chr12:122526924-122527235 | Common:3; Rare:93 | ||||
| chr12:122703309-122703540 | Common:2; Rare:46 | ||||
| chr12:123233119-123233481 | Common:2; Rare:113; Clinvar:1 | ||||
| chr12:123436339-123436751 | Common:1; Rare:101 | ||||
| chr12:123584658-123584811 | Common:3; Rare:43 | ||||
| chr12:123633545-123633840 | Common:1; Rare:140; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124388808-124388962 | Common:3; Rare:44 | ||||
| chr12:124913981-124914251 | Common:7; Rare:98 |