| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101353756-101354189 | Common:1; Rare:132 | ||||
| chr10:101588138-101588349 | Rare:88; Clinvar:1 | ||||
| chr10:101694815-101695075 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101783367-101783457 | Rare:46 | ||||
| chr10:101817825-101817931 | Common:2; Rare:38 | ||||
| chr10:101818335-101818764 | Common:1; Rare:115 | ||||
| chr10:102056089-102056350 | Common:1; Rare:61 | ||||
| chr10:102065173-102065450 | Common:1; Rare:97 | ||||
| chr10:102120428-102120599 | Common:1; Rare:64 | ||||
| chr10:102142925-102143189 | Rare:75 | ||||
| chr10:102152307-102152598 | Common:1; Rare:128 | ||||
| chr10:102159894-102160341 | Rare:117 | ||||
| chr10:102394336-102394586 | Common:1; Rare:67 | ||||
| chr10:102396136-102396235 | Rare:31 | ||||
| chr10:102421091-102421256 | Common:1; Rare:71 |