| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179452307-179452467 | Rare:24 | ||||
| chr3:179483014-179483066 | Rare:6 | ||||
| chr3:179507011-179507076 | Common:1; Rare:6 | ||||
| chr3:179507480-179507544 | Rare:11 | ||||
| chr3:179527000-179527287 | Common:1; Rare:52 | ||||
| chr3:179563479-179563728 | Common:3; Rare:60 | ||||
| chr3:179768009-179768318 | Rare:39 | ||||
| chr3:181293088-181293287 | Rare:29 | ||||
| chr3:181383472-181383669 | Rare:33 | ||||
| chr3:181383807-181384034 | Common:1; Rare:36 | ||||
| chr3:181708148-181708166 | Rare:3 | ||||
| chr3:181710777-181711168 | Common:1; Rare:59 | ||||
| chr3:181712916-181712988 | Rare:16; Clinvar (pathogenic):1 | ||||
| chr3:181715325-181715539 | Rare:43 | ||||
| chr3:181715596-181715672 | Rare:13 |