| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6133447-6133586 | Common:1; Rare:48 | ||||
| chr12:6142834-6142991 | Common:2; Rare:52 | ||||
| chr12:6295069-6295449 | Rare:65 | ||||
| chr12:6573175-6573390 | Rare:45 | ||||
| chr12:6613628-6613690 | Rare:16 | ||||
| chr12:6614142-6614235 | Rare:27 | ||||
| chr12:6708907-6709071 | Common:1; Rare:54 | ||||
| chr12:6716821-6716987 | Common:2; Rare:49 | ||||
| chr12:6764333-6764588 | Rare:64 | ||||
| chr12:6770189-6770485 | Rare:87 | ||||
| chr12:6891081-6891294 | Common:2; Rare:89 | ||||
| chr12:6924973-6925154 | Common:9; Rare:43 | ||||
| chr12:6927575-6927707 | Rare:39 | ||||
| chr12:6935443-6935649 | Common:1; Rare:53 | ||||
| chr12:6974223-6974432 | Rare:64; Clinvar (pathogenic):1 |