| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477293-109477361 | Common:1; Rare:28 | ||||
| chr12:109573483-109573815 | Common:3; Rare:95; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:110450262-110450483 | Common:2; Rare:74 | ||||
| chr12:110468606-110468798 | Rare:49 | ||||
| chr12:110502067-110502331 | Common:1; Rare:94 | ||||
| chr12:110613966-110614132 | Rare:43; Clinvar:2 | ||||
| chr12:110641553-110641846 | Common:1; Rare:63 | ||||
| chr12:110689740-110690038 | Common:1; Rare:47 | ||||
| chr12:111685817-111686129 | Rare:117 | ||||
| chr12:111841915-111842260 | Common:2; Rare:96 | ||||
| chr12:112013128-112013594 | Common:1; Rare:174 | ||||
| chr12:112906933-112907040 | Rare:32 | ||||
| chr12:113185436-113185767 | Common:8; Rare:121 | ||||
| chr12:116738052-116738298 | Common:3; Rare:78 | ||||
| chr12:118136000-118136302 | Common:2; Rare:83 |