| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6635923-6636079 | Common:2; Rare:44 | ||||
| chr12:6723854-6724166 | Common:1; Rare:64 | ||||
| chr12:6752945-6753189 | Common:6; Rare:77 | ||||
| chr12:6851877-6852179 | Rare:81 | ||||
| chr12:6867381-6867680 | Common:2; Rare:142; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873311-6873541 | Common:1; Rare:66 | ||||
| chr12:6967498-6967574 | Rare:28 | ||||
| chr12:6970621-6970961 | Common:3; Rare:107 | ||||
| chr12:7018468-7018542 | Rare:21 | ||||
| chr12:7090055-7090442 | Common:4; Rare:97; Clinvar:2 | ||||
| chr12:7108359-7108681 | Common:2; Rare:102 | ||||
| chr12:7109105-7109399 | Rare:86 | ||||
| chr12:8032401-8032766 | Common:5; Rare:107 | ||||
| chr12:8066335-8066550 | Rare:30 | ||||
| chr12:8697740-8698110 | Common:2; Rare:134 |