| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122266405-122266729 | Common:3; Rare:97 | ||||
| chr12:122526856-122527287 | Common:4; Rare:158 | ||||
| chr12:122872029-122872183 | Rare:21 | ||||
| chr12:122980552-122980965 | Common:2; Rare:120 | ||||
| chr12:123105452-123105661 | Common:1; Rare:37 | ||||
| chr12:123233109-123233497 | Common:2; Rare:129; Clinvar:1 | ||||
| chr12:123364816-123364974 | Common:2; Rare:61 | ||||
| chr12:123584297-123584652 | Common:6; Rare:127 | ||||
| chr12:123601840-123602181 | Common:6; Rare:97 | ||||
| chr12:123633620-123633851 | Common:1; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972565-123972909 | Common:6; Rare:118 | ||||
| chr12:124422655-124422916 | Common:4; Rare:67 | ||||
| chr12:124786464-124786786 | Common:3; Rare:87 | ||||
| chr12:124914805-124915066 | Common:3; Rare:107 | ||||
| chr12:130871730-130872126 | Common:4; Rare:165 |