| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122858945-122859191 | Common:3; Rare:93 | ||||
| chr12:122896048-122896226 | Rare:94 | ||||
| chr12:122974544-122974758 | Common:1; Rare:56 | ||||
| chr12:122975151-122975252 | Common:1; Rare:31 | ||||
| chr12:122980568-122980823 | Common:1; Rare:88 | ||||
| chr12:123233087-123233490 | Common:2; Rare:134; Clinvar:1 | ||||
| chr12:123364800-123364977 | Common:3; Rare:71 | ||||
| chr12:123383804-123384159 | Rare:73 | ||||
| chr12:123436141-123436249 | Rare:26 | ||||
| chr12:123436360-123436549 | Rare:42 | ||||
| chr12:123436553-123436867 | Common:2; Rare:72 | ||||
| chr12:123457838-123458196 | Common:1; Rare:67 | ||||
| chr12:123584317-123584645 | Common:6; Rare:117 | ||||
| chr12:123602023-123602174 | Common:3; Rare:56 | ||||
| chr12:123633602-123633851 | Common:1; Rare:120; Clinvar:8; Clinvar (benign):1 |