| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101817138-101817397 | Common:1; Rare:59 | ||||
| chr10:101817506-101817739 | Common:1; Rare:48 | ||||
| chr10:101818096-101818211 | Rare:37 | ||||
| chr10:101818341-101818883 | Common:1; Rare:138 | ||||
| chr10:101818949-101819086 | Common:1; Rare:29 | ||||
| chr10:102055854-102056051 | Common:1; Rare:54 | ||||
| chr10:102056099-102056412 | Common:3; Rare:74 | ||||
| chr10:102064977-102065029 | Rare:7 | ||||
| chr10:102065204-102065480 | Common:1; Rare:104 | ||||
| chr10:102065844-102065892 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr10:102114497-102114514 | Rare:2 | ||||
| chr10:102114894-102115143 | Common:3; Rare:64 | ||||
| chr10:102120417-102120690 | Common:1; Rare:97 | ||||
| chr10:102120692-102120806 | Rare:37 | ||||
| chr10:102132539-102132697 | Rare:34 |