| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14178306-14178425 | Rare:37 | ||||
| chr3:14178491-14178931 | Common:3; Rare:216; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402383-14402742 | Common:3; Rare:85 | ||||
| chr3:14402774-14403042 | Common:3; Rare:58 | ||||
| chr3:14431985-14432582 | Common:2; Rare:106 | ||||
| chr3:14432585-14432755 | Common:2; Rare:32 | ||||
| chr3:14651378-14651867 | Common:1; Rare:153 | ||||
| chr3:14947086-14947157 | Rare:27 | ||||
| chr3:14947333-14947634 | Common:4; Rare:135 | ||||
| chr3:14947938-14948263 | Rare:145 | ||||
| chr3:14948403-14948740 | Common:3; Rare:110 | ||||
| chr3:15050543-15050742 | Common:1; Rare:42 | ||||
| chr3:15064774-15064914 | Rare:38 | ||||
| chr3:15065164-15065440 | Common:5; Rare:100 | ||||
| chr3:15098803-15098958 | Rare:23 |