| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102114944-102115061 | Common:1; Rare:41 | ||||
| chr10:102120458-102120592 | Common:1; Rare:44 | ||||
| chr10:102152030-102152476 | Common:4; Rare:146 | ||||
| chr10:102226140-102226301 | Common:1; Rare:35 | ||||
| chr10:102394358-102394495 | Rare:38 | ||||
| chr10:102420975-102421230 | Rare:102 | ||||
| chr10:102432546-102432797 | Common:1; Rare:73 | ||||
| chr10:102461205-102461434 | Rare:61 | ||||
| chr10:102502657-102502871 | Rare:74 | ||||
| chr10:102714271-102714659 | Common:2; Rare:127 | ||||
| chr10:102743759-102744014 | Common:2; Rare:63 | ||||
| chr10:102776099-102776241 | Common:1; Rare:25 | ||||
| chr10:102854173-102854292 | Common:1; Rare:39 | ||||
| chr10:102917992-102918306 | Common:1; Rare:97 | ||||
| chr10:103193248-103193380 | Common:5; Rare:44; Clinvar (benign):1 |