| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120201081-120201354 | Common:2; Rare:88 | ||||
| chr12:120446344-120446474 | Common:1; Rare:58 | ||||
| chr12:120469482-120469912 | Common:5; Rare:144 | ||||
| chr12:120495867-120496252 | Common:7; Rare:129 | ||||
| chr12:120529094-120529334 | Common:2; Rare:74 | ||||
| chr12:120534308-120534356 | Rare:22 | ||||
| chr12:120581360-120581547 | Common:1; Rare:72 | ||||
| chr12:120686945-120687189 | Common:2; Rare:87 | ||||
| chr12:120687392-120687536 | Rare:34 | ||||
| chr12:120725720-120725888 | Rare:55; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:121210046-121210167 | Common:2; Rare:43 | ||||
| chr12:121399870-121400165 | Common:5; Rare:109 | ||||
| chr12:121536058-121536138 | Rare:14 | ||||
| chr12:121672624-121672780 | Common:4; Rare:54 | ||||
| chr12:121712641-121712845 | Common:3; Rare:79 |