| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57240650-57240940 | Common:1; Rare:79 | ||||
| chr12:57430193-57430305 | Rare:27 | ||||
| chr12:57430521-57430686 | Rare:45 | ||||
| chr12:57430600-57431301 | Common:12; Rare:467 | ||||
| chr12:57454969-57455544 | Rare:162 | ||||
| chr12:57487740-57488435 | Common:4; Rare:228; Clinvar:5; Clinvar (benign):3 | ||||
| chr12:57488510-57489100 | Common:8; Rare:208; Clinvar (benign):4 | ||||
| chr12:57520372-57520842 | Common:7; Rare:287 | ||||
| chr12:57520750-57521159 | Common:2; Rare:152 | ||||
| chr12:57521763-57521866 | Common:1; Rare:19 | ||||
| chr12:57522372-57523263 | Common:11; Rare:524 | ||||
| chr12:57546497-57546643 | Rare:29 | ||||
| chr12:57547095-57547352 | Common:2; Rare:102 | ||||
| chr12:57590991-57591466 | Common:18; Rare:456 | ||||
| chr12:57591602-57592251 | Common:6; Rare:172 |