| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113746983-113747076 | Common:3; Rare:12 | ||||
| chr3:114056475-114056823 | Common:2; Rare:134 | ||||
| chr3:119468916-119469004 | Rare:43 | ||||
| chr3:119498406-119498625 | Common:3; Rare:75 | ||||
| chr3:119677367-119677505 | Common:1; Rare:46 | ||||
| chr3:120596122-120596362 | Common:2; Rare:84 | ||||
| chr3:120682195-120682331 | Rare:33; Clinvar:4 | ||||
| chr3:120742511-120742771 | Common:2; Rare:72 | ||||
| chr3:121749137-121749293 | Rare:27 | ||||
| chr3:121749643-121749991 | Common:1; Rare:79 | ||||
| chr3:121834987-121835244 | Common:3; Rare:87; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383199-122383310 | Common:1; Rare:34 | ||||
| chr3:122384068-122384268 | Rare:75 | ||||
| chr3:122514873-122515006 | Common:1; Rare:38 | ||||
| chr3:122564243-122564437 | Common:3; Rare:58 |