| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:87227244-87227386 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058946-88059289 | Common:2; Rare:123 | ||||
| chr3:88149862-88150010 | Rare:48 | ||||
| chr3:97764516-97764796 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr3:97821946-97822076 | Rare:50 | ||||
| chr3:99638389-99638624 | Common:1; Rare:57 | ||||
| chr3:99817562-99817934 | Rare:112 | ||||
| chr3:99876096-99876269 | Common:1; Rare:49 | ||||
| chr3:100260711-100261048 | Rare:97 | ||||
| chr3:101513126-101513375 | Common:8; Rare:64 | ||||
| chr3:101561746-101561956 | Common:2; Rare:78 | ||||
| chr3:101574007-101574245 | Rare:86 | ||||
| chr3:101686680-101686860 | Common:2; Rare:77 | ||||
| chr3:101724530-101724638 | Rare:34 | ||||
| chr3:101779092-101779248 | Common:3; Rare:48 |