| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38029636-38029844 | Common:1; Rare:42 | ||||
| chr3:39051944-39052050 | Common:1; Rare:39 | ||||
| chr3:39107562-39107696 | Common:3; Rare:42 | ||||
| chr3:39383258-39383437 | Common:2; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383582-39383651 | Rare:16 | ||||
| chr3:39406574-39406758 | Common:2; Rare:79 | ||||
| chr3:40309496-40309808 | Common:9; Rare:108 | ||||
| chr3:40457204-40457370 | Common:2; Rare:79 | ||||
| chr3:40524839-40525013 | Rare:48 | ||||
| chr3:42581913-42582081 | Common:2; Rare:58 | ||||
| chr3:42600328-42600761 | Common:3; Rare:169 | ||||
| chr3:42600870-42601000 | Rare:47 | ||||
| chr3:42630724-42631045 | Common:1; Rare:60 | ||||
| chr3:42804427-42804657 | Common:2; Rare:68 | ||||
| chr3:43621919-43622257 | Common:2; Rare:106; Clinvar:7; Clinvar (benign):1 |