| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:35638457-35638632 | Common:1; Rare:30 | ||||
| chr3:35638838-35638859 | Rare:3 | ||||
| chr3:35638860-35638979 | Rare:24 | ||||
| chr3:35639416-35639848 | Common:4; Rare:96 | ||||
| chr3:35639850-35640125 | Common:2; Rare:70 | ||||
| chr3:36993108-36993553 | Common:2; Rare:141; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr3:37176147-37176393 | Rare:65 | ||||
| chr3:37243166-37243316 | Common:1; Rare:37 | ||||
| chr3:39051939-39052085 | Common:1; Rare:54 | ||||
| chr3:39107597-39107681 | Common:2; Rare:26 | ||||
| chr3:39383289-39383432 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39406573-39406758 | Common:2; Rare:79 | ||||
| chr3:40309470-40309904 | Common:9; Rare:143 | ||||
| chr3:40310365-40310494 | Common:2; Rare:20 | ||||
| chr3:40457204-40457370 | Common:2; Rare:79 |