| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100912675-100913086 | Common:1; Rare:120 | ||||
| chr10:100987414-100987573 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996983-100997117 | Common:1; Rare:42 | ||||
| chr10:100999608-100999930 | Common:2; Rare:95 | ||||
| chr10:101031136-101031292 | Rare:35 | ||||
| chr10:101588180-101588330 | Rare:62 | ||||
| chr10:101818340-101818770 | Common:1; Rare:115 | ||||
| chr10:102056100-102056366 | Common:1; Rare:64 | ||||
| chr10:102114966-102115104 | Common:2; Rare:43 | ||||
| chr10:102152052-102152402 | Common:3; Rare:104 | ||||
| chr10:102394324-102394582 | Common:1; Rare:69 | ||||
| chr10:102395551-102395735 | Common:1; Rare:51 | ||||
| chr10:102432546-102432835 | Common:2; Rare:86 | ||||
| chr10:102644993-102645126 | Rare:31 | ||||
| chr10:102714244-102714636 | Common:2; Rare:133 |