| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37628975-37629256 | Rare:85 | ||||
| chr3:37693504-37693772 | Common:1; Rare:48 | ||||
| chr3:37694347-37694614 | Rare:63 | ||||
| chr3:38455423-38455566 | Common:1; Rare:32 | ||||
| chr3:39013398-39013555 | Common:1; Rare:20 | ||||
| chr3:39384258-39384541 | Common:10; Rare:71 | ||||
| chr3:40230076-40230302 | Common:1; Rare:37 | ||||
| chr3:40453155-40453417 | Common:6; Rare:58 | ||||
| chr3:41117502-41117817 | Common:2; Rare:74 | ||||
| chr3:41200822-41201209 | Common:5; Rare:80 | ||||
| chr3:41203061-41203131 | Rare:13 | ||||
| chr3:41225329-41225801 | Rare:97; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:41276132-41276697 | Common:3; Rare:113 | ||||
| chr3:42036549-42036682 | Rare:19 | ||||
| chr3:43954086-43954267 | Rare:39 |