| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4649026-4649154 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr12:6493235-6493502 | Common:7; Rare:79 | ||||
| chr12:6493746-6494153 | Common:2; Rare:120 | ||||
| chr12:6534245-6534582 | Common:6; Rare:133 | ||||
| chr12:6568260-6568356 | Rare:36 | ||||
| chr12:6663102-6663403 | Common:2; Rare:83 | ||||
| chr12:6688897-6689089 | Rare:63 | ||||
| chr12:6723970-6724123 | Rare:35 | ||||
| chr12:6753066-6753189 | Common:4; Rare:47 | ||||
| chr12:6851894-6852174 | Rare:72 | ||||
| chr12:6867355-6867545 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6914407-6914659 | Common:2; Rare:66 | ||||
| chr12:6943525-6943818 | Common:4; Rare:122 | ||||
| chr12:6970624-6970955 | Common:3; Rare:103 | ||||
| chr12:7018468-7018571 | Common:1; Rare:30 |