| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109999118-109999211 | Rare:13 | ||||
| chr12:110280989-110281193 | Common:1; Rare:83 | ||||
| chr12:110386935-110387155 | Common:1; Rare:40 | ||||
| chr12:110468715-110468909 | Rare:52 | ||||
| chr12:110502051-110502195 | Common:1; Rare:53 | ||||
| chr12:110613997-110614246 | Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742655-110742727 | Common:1; Rare:17; Clinvar:1 | ||||
| chr12:111369025-111369262 | Common:1; Rare:64 | ||||
| chr12:111599338-111599635 | Common:2; Rare:97 | ||||
| chr12:111685704-111686138 | Rare:154 | ||||
| chr12:111766814-111767013 | Rare:66 | ||||
| chr12:111841887-111842048 | Common:2; Rare:46 | ||||
| chr12:112013119-112013501 | Common:1; Rare:144 | ||||
| chr12:112013510-112013611 | Rare:37 | ||||
| chr12:112108748-112108918 | Common:1; Rare:45 |