| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32755878-32756015 | Rare:45 | ||||
| chr12:32896755-32897011 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905569-38905742 | Common:3; Rare:44 | ||||
| chr12:38906261-38906542 | Common:2; Rare:58 | ||||
| chr12:39442977-39443072 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:42238153-42238483 | Common:1; Rare:108 | ||||
| chr12:42325998-42326211 | Common:1; Rare:69 | ||||
| chr12:43758745-43758996 | Common:2; Rare:69; Clinvar:2 | ||||
| chr12:45215963-45216174 | Common:3; Rare:69 | ||||
| chr12:45990390-45990940 | Common:2; Rare:178 | ||||
| chr12:45992030-45992293 | Common:2; Rare:42 | ||||
| chr12:46362277-46362635 | Common:2; Rare:92 | ||||
| chr12:46367063-46367337 | Common:2; Rare:76 | ||||
| chr12:46372513-46372986 | Rare:162 | ||||
| chr12:47079511-47079639 | Common:1; Rare:26 |