| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867778-6867961 | Common:3; Rare:40 | ||||
| chr12:6867988-6868122 | Common:2; Rare:55 | ||||
| chr12:6873232-6873743 | Common:5; Rare:140 | ||||
| chr12:6873830-6873931 | Rare:13 | ||||
| chr12:6904627-6905117 | Common:3; Rare:107 | ||||
| chr12:6914436-6914612 | Rare:48 | ||||
| chr12:6927556-6928043 | Common:1; Rare:127 | ||||
| chr12:6928328-6928463 | Common:1; Rare:31 | ||||
| chr12:6928497-6928532 | Rare:6 | ||||
| chr12:6937525-6937776 | Common:2; Rare:71 | ||||
| chr12:6937807-6938268 | Common:2; Rare:176; Clinvar (benign):1 | ||||
| chr12:6943471-6943889 | Common:8; Rare:237 | ||||
| chr12:6943899-6944260 | Common:12; Rare:329; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6944441-6944725 | Common:2; Rare:114; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr12:6946227-6946739 | Common:2; Rare:145 |