| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120742160-120742420 | Common:1; Rare:106 | ||||
| chr3:120742438-120742899 | Common:15; Rare:642 | ||||
| chr3:120743057-120743457 | Rare:82 | ||||
| chr3:121545116-121545516 | Common:1; Rare:63 | ||||
| chr3:121545869-121546260 | Common:10; Rare:346 | ||||
| chr3:121546396-121547108 | Common:5; Rare:174 | ||||
| chr3:121660448-121661147 | Rare:258 | ||||
| chr3:121748734-121749451 | Rare:297 | ||||
| chr3:121749643-121750198 | Common:14; Rare:659 | ||||
| chr3:121834908-121835346 | Common:23; Rare:734; Clinvar:42; Clinvar (benign):14 | ||||
| chr3:122325005-122325248 | Common:3; Rare:47 | ||||
| chr3:122382967-122383456 | Common:11; Rare:424 | ||||
| chr3:122383949-122384734 | Common:14; Rare:736 | ||||
| chr3:122415969-122416330 | Common:5; Rare:587 | ||||
| chr3:122416367-122416767 | Common:5; Rare:127 |