| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100356236-100356851 | Common:9; Rare:168 | ||||
| chr10:100371328-100371474 | Rare:71 | ||||
| chr10:100373286-100373725 | Common:6; Rare:158 | ||||
| chr10:100373757-100373880 | Common:1; Rare:19 | ||||
| chr10:100373930-100374372 | Rare:134 | ||||
| chr10:100878280-100878418 | Rare:30 | ||||
| chr10:100970102-100970415 | Rare:156 | ||||
| chr10:101010820-101011300 | Common:11; Rare:132; Clinvar (benign):2 | ||||
| chr10:101031973-101032104 | Rare:32 | ||||
| chr10:101042860-101043270 | Rare:132 | ||||
| chr10:101060670-101060910 | Common:1; Rare:84 | ||||
| chr10:101060975-101061289 | Common:4; Rare:189 | ||||
| chr10:101693780-101694440 | Common:1; Rare:210; Clinvar:2 | ||||
| chr10:102058047-102058447 | Common:6; Rare:219 | ||||
| chr10:102065970-102066440 | Common:1; Rare:351; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):2 |