| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6821397-6821503 | Rare:22 | ||||
| chr12:6821693-6821893 | Common:1; Rare:52 | ||||
| chr12:6828287-6828668 | Common:4; Rare:85 | ||||
| chr12:6828792-6828831 | Rare:7 | ||||
| chr12:6829395-6829459 | Rare:19 | ||||
| chr12:6829628-6829702 | Rare:14 | ||||
| chr12:6850602-6850902 | Common:1; Rare:62 | ||||
| chr12:6851217-6851521 | Rare:72 | ||||
| chr12:6851877-6852195 | Rare:85 | ||||
| chr12:6852265-6852686 | Common:1; Rare:108 | ||||
| chr12:6867313-6867658 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6867957-6868333 | Common:7; Rare:122 | ||||
| chr12:6873281-6873409 | Common:2; Rare:35 | ||||
| chr12:6904636-6905067 | Common:3; Rare:94 | ||||
| chr12:6913823-6913913 | Rare:26 |