| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101839813-101839924 | Rare:34 | ||||
| chr10:102056100-102056368 | Common:1; Rare:64 | ||||
| chr10:102114948-102115133 | Common:2; Rare:54 | ||||
| chr10:102152029-102152406 | Common:3; Rare:115 | ||||
| chr10:102394335-102394570 | Rare:64 | ||||
| chr10:102419091-102419229 | Rare:29 | ||||
| chr10:102432524-102432781 | Common:1; Rare:74 | ||||
| chr10:102461301-102461435 | Rare:40 | ||||
| chr10:102502643-102502925 | Common:1; Rare:91 | ||||
| chr10:102714197-102714645 | Common:2; Rare:148 | ||||
| chr10:102776041-102776224 | Common:1; Rare:27 | ||||
| chr10:102853988-102854315 | Common:2; Rare:104 | ||||
| chr10:103276942-103277157 | Common:1; Rare:55 | ||||
| chr10:103277581-103277952 | Common:1; Rare:95; Clinvar (pathogenic):1 | ||||
| chr10:103350905-103351188 | Common:2; Rare:116 |