| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477260-109477653 | Common:3; Rare:103 | ||||
| chr12:109573483-109573813 | Common:3; Rare:95; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:109900195-109900302 | Rare:46 | ||||
| chr12:110468719-110468909 | Rare:52 | ||||
| chr12:110502058-110502198 | Common:1; Rare:52 | ||||
| chr12:111685806-111686113 | Rare:118 | ||||
| chr12:111841921-111841989 | Common:1; Rare:21 | ||||
| chr12:112013147-112013460 | Common:1; Rare:109 | ||||
| chr12:113185447-113185511 | Common:3; Rare:25 | ||||
| chr12:118135955-118136183 | Common:2; Rare:69 | ||||
| chr12:120201085-120201354 | Common:2; Rare:86 | ||||
| chr12:120446359-120446474 | Common:1; Rare:51 | ||||
| chr12:120469555-120469873 | Common:2; Rare:113 | ||||
| chr12:120495875-120496152 | Common:5; Rare:88 | ||||
| chr12:120529118-120529250 | Common:1; Rare:44 |