| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851651-6851743 | Common:2; Rare:15 | ||||
| chr12:6851859-6852195 | Rare:96 | ||||
| chr12:6852279-6852721 | Common:1; Rare:118 | ||||
| chr12:6867313-6867658 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6867960-6868318 | Common:7; Rare:118 | ||||
| chr12:6873244-6873651 | Common:4; Rare:119 | ||||
| chr12:6904676-6904947 | Common:2; Rare:63 | ||||
| chr12:6914391-6914871 | Common:3; Rare:107 | ||||
| chr12:6915416-6915507 | Common:1; Rare:10 | ||||
| chr12:6922114-6922387 | Rare:55 | ||||
| chr12:6924379-6924538 | Common:1; Rare:37 | ||||
| chr12:6927763-6927914 | Rare:44 | ||||
| chr12:6928258-6928440 | Common:1; Rare:39 | ||||
| chr12:6937554-6937707 | Common:1; Rare:35 | ||||
| chr12:6937793-6938262 | Common:2; Rare:176; Clinvar (benign):1 |