| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102420736-102420855 | Rare:25 | ||||
| chr10:102420895-102421266 | Common:1; Rare:129 | ||||
| chr10:102432033-102432179 | Common:1; Rare:27 | ||||
| chr10:102432185-102432236 | Rare:7 | ||||
| chr10:102432488-102432859 | Common:2; Rare:100 | ||||
| chr10:102461019-102461489 | Common:1; Rare:116 | ||||
| chr10:102501986-102502348 | Common:3; Rare:114 | ||||
| chr10:102502536-102502968 | Common:2; Rare:122 | ||||
| chr10:102503724-102504100 | Common:4; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:102644161-102644509 | Common:2; Rare:102 | ||||
| chr10:102645044-102645199 | Rare:32 | ||||
| chr10:102713821-102714055 | Rare:45 | ||||
| chr10:102714173-102714684 | Common:2; Rare:162 | ||||
| chr10:102714857-102714896 | Rare:4 | ||||
| chr10:102715109-102715171 | Rare:13 |