| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100969247-100969546 | Common:3; Rare:75 | ||||
| chr10:100987228-100987599 | Common:1; Rare:134; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101031093-101031310 | Common:1; Rare:48 | ||||
| chr10:101229433-101229467 | Rare:6 | ||||
| chr10:101588166-101588342 | Rare:73 | ||||
| chr10:101818114-101818237 | Rare:46 | ||||
| chr10:101818397-101818817 | Common:1; Rare:110 | ||||
| chr10:101839802-101839908 | Rare:37 | ||||
| chr10:102056100-102056387 | Common:2; Rare:70 | ||||
| chr10:102114932-102115140 | Common:2; Rare:59 | ||||
| chr10:102152144-102152406 | Common:3; Rare:90 | ||||
| chr10:102394329-102394531 | Rare:55 | ||||
| chr10:102418750-102419050 | Rare:62 | ||||
| chr10:102419091-102419229 | Rare:29 | ||||
| chr10:102419656-102419838 | Rare:53 |