| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108731456-108731640 | Common:2; Rare:66 | ||||
| chr12:109093621-109093903 | Common:2; Rare:63 | ||||
| chr12:109097847-109098250 | Common:5; Rare:126 | ||||
| chr12:109477275-109477664 | Common:3; Rare:101 | ||||
| chr12:109573421-109573845 | Common:5; Rare:142; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880312-109880678 | Common:1; Rare:113 | ||||
| chr12:109900159-109900348 | Rare:66 | ||||
| chr12:109996257-109996452 | Common:2; Rare:57 | ||||
| chr12:109999108-109999211 | Rare:15 | ||||
| chr12:110280990-110281193 | Common:1; Rare:83 | ||||
| chr12:110450265-110450437 | Common:2; Rare:61 | ||||
| chr12:110468665-110468909 | Rare:62 | ||||
| chr12:110502058-110502200 | Common:1; Rare:54 | ||||
| chr12:110614004-110614187 | Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685761-111686110 | Rare:130 |