| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113422318-113422425 | Common:1; Rare:24 | ||||
| chr12:113966208-113966548 | Common:10; Rare:112 | ||||
| chr12:114684146-114684353 | Rare:54 | ||||
| chr12:114684392-114684632 | Common:2; Rare:64 | ||||
| chr12:116738101-116738356 | Common:3; Rare:72 | ||||
| chr12:116910864-116911025 | Rare:56 | ||||
| chr12:118061059-118061466 | Common:4; Rare:89 | ||||
| chr12:118062410-118062478 | Rare:12 | ||||
| chr12:118103876-118104147 | Common:1; Rare:62 | ||||
| chr12:118135938-118136201 | Common:2; Rare:83 | ||||
| chr12:118372866-118373192 | Common:1; Rare:86 | ||||
| chr12:118376454-118376781 | Common:1; Rare:102 | ||||
| chr12:119178501-119179041 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119179576-119179872 | Common:1; Rare:70; Clinvar:2 | ||||
| chr12:119877261-119877550 | Common:2; Rare:68 |