| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100913328-100913436 | Rare:30 | ||||
| chr10:100969217-100969519 | Common:3; Rare:78 | ||||
| chr10:100987091-100987336 | Rare:86 | ||||
| chr10:100987342-100987581 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100999254-100999329 | Rare:16 | ||||
| chr10:101031139-101031533 | Rare:88 | ||||
| chr10:101588205-101588348 | Rare:58; Clinvar:1 | ||||
| chr10:101818323-101818770 | Common:1; Rare:122 | ||||
| chr10:102056100-102056368 | Common:1; Rare:64 | ||||
| chr10:102110628-102110893 | Rare:74 | ||||
| chr10:102120435-102120565 | Common:1; Rare:50 | ||||
| chr10:102394196-102394570 | Rare:99 | ||||
| chr10:102395561-102395729 | Common:1; Rare:47 | ||||
| chr10:102714262-102714645 | Common:2; Rare:129 | ||||
| chr10:102776030-102776279 | Common:1; Rare:44 |