| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120742493-120742836 | Common:2; Rare:93 | ||||
| chr3:121749642-121750011 | Common:1; Rare:85 | ||||
| chr3:121834966-121835245 | Common:3; Rare:92; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383149-122383332 | Common:1; Rare:56 | ||||
| chr3:122384103-122384293 | Common:3; Rare:71 | ||||
| chr3:122416001-122416229 | Common:1; Rare:75 | ||||
| chr3:122514760-122515021 | Common:3; Rare:73 | ||||
| chr3:122564238-122564422 | Common:3; Rare:54 | ||||
| chr3:122564501-122564604 | Rare:29 | ||||
| chr3:122681033-122681233 | Rare:57 | ||||
| chr3:122793682-122793902 | Common:3; Rare:67 | ||||
| chr3:122795002-122795138 | Common:2; Rare:63 | ||||
| chr3:122795475-122795490 | Rare:3 | ||||
| chr3:123067006-123067162 | Rare:38 | ||||
| chr3:123585020-123585305 | Common:1; Rare:90 |