| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109996196-109996450 | Common:2; Rare:72 | ||||
| chr12:109999071-109999224 | Rare:28 | ||||
| chr12:110280442-110280653 | Rare:48 | ||||
| chr12:110280679-110280722 | Rare:8 | ||||
| chr12:110280902-110281196 | Common:1; Rare:105 | ||||
| chr12:110450235-110450466 | Common:2; Rare:84 | ||||
| chr12:110468659-110468909 | Rare:63 | ||||
| chr12:110502047-110502242 | Common:1; Rare:68 | ||||
| chr12:110614008-110614303 | Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742709-110743197 | Common:3; Rare:172 | ||||
| chr12:111599328-111599646 | Common:2; Rare:101 | ||||
| chr12:111685765-111686127 | Rare:135 | ||||
| chr12:111766795-111767007 | Rare:69 | ||||
| chr12:111841845-111842251 | Common:3; Rare:115 | ||||
| chr12:112013113-112013490 | Common:1; Rare:140 |