| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179605046-179605184 | Common:1; Rare:30 | ||||
| chr3:179974186-179974342 | Common:2; Rare:18 | ||||
| chr3:180602017-180602281 | Common:1; Rare:89 | ||||
| chr3:180679357-180679568 | Rare:56; Clinvar:3 | ||||
| chr3:180868128-180868191 | Rare:14 | ||||
| chr3:180868700-180868789 | Rare:17 | ||||
| chr3:180870114-180870187 | Common:1; Rare:19 | ||||
| chr3:180870507-180870633 | Common:1; Rare:19 | ||||
| chr3:180870947-180871121 | Common:1; Rare:26 | ||||
| chr3:180912370-180912548 | Common:3; Rare:53 | ||||
| chr3:180912597-180912736 | Common:1; Rare:48 | ||||
| chr3:180989572-180989815 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:181711760-181711985 | Rare:67 | ||||
| chr3:182793360-182793745 | Common:3; Rare:111 | ||||
| chr3:182980487-182980799 | Common:3; Rare:106 |