| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31959269-31959488 | Common:2; Rare:73 | ||||
| chr12:32399750-32399885 | Common:1; Rare:52 | ||||
| chr12:32502102-32502218 | Common:1; Rare:23; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:32755884-32755980 | Rare:34 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905588-38905694 | Common:3; Rare:28 | ||||
| chr12:42238193-42238447 | Rare:85 | ||||
| chr12:42325964-42326215 | Common:1; Rare:80 | ||||
| chr12:43758738-43758996 | Common:2; Rare:72; Clinvar:2 | ||||
| chr12:45216007-45216204 | Rare:58 | ||||
| chr12:45990499-45990688 | Common:1; Rare:62 | ||||
| chr12:46372557-46372955 | Rare:151 | ||||
| chr12:47079511-47079651 | Common:1; Rare:27 | ||||
| chr12:47223423-47223562 | Rare:26 | ||||
| chr12:47705972-47706124 | Rare:67 |