| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102854243-102854285 | Rare:21 | ||||
| chr10:102869363-102869568 | Common:5; Rare:51 | ||||
| chr10:103193248-103193506 | Common:5; Rare:78; Clinvar (benign):1 | ||||
| chr10:103396411-103396722 | Rare:108 | ||||
| chr10:104121825-104122174 | Common:2; Rare:116 | ||||
| chr10:104268885-104269185 | Common:3; Rare:70 | ||||
| chr10:109923422-109923631 | Common:2; Rare:74 | ||||
| chr10:110007668-110008265 | Common:2; Rare:194 | ||||
| chr10:110567381-110567803 | Common:2; Rare:129; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110871652-110871957 | Rare:97 | ||||
| chr10:110919339-110919629 | Common:7; Rare:79 | ||||
| chr10:112183681-112183818 | Common:2; Rare:46 | ||||
| chr10:112446877-112447386 | Common:3; Rare:134 | ||||
| chr10:113854369-113854879 | Common:1; Rare:114 | ||||
| chr10:116670248-116670442 | Common:2; Rare:43 |