| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124685-14125179 | Common:4; Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178878 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402405-14402632 | Common:1; Rare:61 | ||||
| chr3:14651486-14651818 | Rare:98 | ||||
| chr3:14947343-14947569 | Common:3; Rare:106 | ||||
| chr3:14948017-14948177 | Rare:78 | ||||
| chr3:15065073-15065364 | Common:2; Rare:107 | ||||
| chr3:15099102-15099293 | Rare:48 | ||||
| chr3:15206064-15206278 | Rare:85 | ||||
| chr3:15427465-15427629 | Common:1; Rare:58 | ||||
| chr3:15601498-15601810 | Common:4; Rare:131; Clinvar:2 | ||||
| chr3:15859800-15860089 | Common:4; Rare:89 | ||||
| chr3:16264881-16265243 | Common:2; Rare:119 | ||||
| chr3:16513456-16513865 | Common:4; Rare:113 | ||||
| chr3:16884227-16884770 | Common:5; Rare:121 |