| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100987437-100987582 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101031107-101031275 | Common:1; Rare:40 | ||||
| chr10:101588161-101588333 | Rare:71 | ||||
| chr10:101694865-101695008 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101818267-101818762 | Common:1; Rare:134 | ||||
| chr10:102056100-102056368 | Common:1; Rare:64 | ||||
| chr10:102160259-102160520 | Common:2; Rare:73 | ||||
| chr10:102226104-102226328 | Common:2; Rare:56 | ||||
| chr10:102245217-102245581 | Common:1; Rare:66 | ||||
| chr10:102394348-102394570 | Rare:60 | ||||
| chr10:102395558-102395735 | Common:1; Rare:49 | ||||
| chr10:102432530-102432787 | Common:1; Rare:78 | ||||
| chr10:102714194-102714669 | Common:2; Rare:154 | ||||
| chr10:102776041-102776282 | Common:1; Rare:39 | ||||
| chr10:102854052-102854289 | Common:1; Rare:80 |