| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57250972-57251313 | Common:1; Rare:85 | ||||
| chr12:57430774-57431119 | Common:1; Rare:96 | ||||
| chr12:57454524-57454727 | Rare:43 | ||||
| chr12:57454971-57455344 | Rare:68 | ||||
| chr12:57459778-57459905 | Common:1; Rare:28 | ||||
| chr12:57459955-57460198 | Common:2; Rare:62 | ||||
| chr12:57488775-57489032 | Common:3; Rare:51; Clinvar (benign):1 | ||||
| chr12:57522520-57522896 | Common:3; Rare:144 | ||||
| chr12:57591113-57591389 | Common:4; Rare:117 | ||||
| chr12:57604797-57604858 | Rare:10 | ||||
| chr12:57611221-57611528 | Common:1; Rare:60 | ||||
| chr12:57611657-57611980 | Common:3; Rare:91 | ||||
| chr12:57614618-57614883 | Rare:62 | ||||
| chr12:57633093-57633276 | Rare:57 | ||||
| chr12:57715846-57716512 | Common:7; Rare:195 |