| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102409274-102409420 | Rare:29 | ||||
| chr10:102420727-102420870 | Rare:30 | ||||
| chr10:102420961-102421280 | Common:1; Rare:117 | ||||
| chr10:102421352-102421652 | Common:1; Rare:94 | ||||
| chr10:102432483-102432841 | Common:2; Rare:97 | ||||
| chr10:102461045-102461518 | Common:1; Rare:115 | ||||
| chr10:102501974-102502332 | Common:3; Rare:113 | ||||
| chr10:102502628-102502969 | Common:1; Rare:101 | ||||
| chr10:102503735-102504044 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:102644184-102644495 | Common:1; Rare:90 | ||||
| chr10:102644889-102645032 | Rare:32 | ||||
| chr10:102713854-102714007 | Rare:26 | ||||
| chr10:102714014-102714174 | Rare:33 | ||||
| chr10:102714182-102714724 | Common:3; Rare:169 | ||||
| chr10:102714826-102714929 | Common:1; Rare:16 |