| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498367-119498620 | Common:4; Rare:88 | ||||
| chr3:120742503-120742789 | Common:2; Rare:81 | ||||
| chr3:121834989-121835238 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122384054-122384281 | Common:3; Rare:81 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122514798-122515029 | Common:3; Rare:63 | ||||
| chr3:122564176-122564348 | Common:3; Rare:41 | ||||
| chr3:123692341-123692460 | Rare:28 | ||||
| chr3:126083969-126084200 | Common:2; Rare:65 | ||||
| chr3:127598255-127598440 | Common:2; Rare:47 | ||||
| chr3:128052149-128052546 | Common:3; Rare:134 | ||||
| chr3:129183814-129184075 | Common:2; Rare:89 | ||||
| chr3:129249512-129249712 | Common:2; Rare:61 | ||||
| chr3:129316283-129316338 | Rare:21 | ||||
| chr3:129439836-129440212 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 |