| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142447964-142448122 | Common:1; Rare:56 | ||||
| chr3:142578716-142579011 | Rare:102; Clinvar:1 | ||||
| chr3:143001427-143001654 | Common:3; Rare:87 | ||||
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:149129545-149129701 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377449-149377704 | Common:1; Rare:78 | ||||
| chr3:149657943-149658181 | Rare:49 | ||||
| chr3:149812999-149813291 | Common:2; Rare:98 | ||||
| chr3:149970864-149971104 | Common:1; Rare:112 | ||||
| chr3:150408069-150408326 | Common:2; Rare:91 | ||||
| chr3:150603141-150603404 | Common:2; Rare:104 | ||||
| chr3:150763161-150763448 | Common:1; Rare:68 | ||||
| chr3:151316603-151316895 | Common:2; Rare:59 | ||||
| chr3:152268513-152269342 | Common:2; Rare:283 | ||||
| chr3:152269509-152269759 | Common:2; Rare:74 |