| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95756473-95756564 | Common:1; Rare:26 | ||||
| chr10:95907766-95907923 | Common:1; Rare:43 | ||||
| chr10:96129970-96130686 | Common:5; Rare:230 | ||||
| chr10:96586963-96587211 | Rare:99 | ||||
| chr10:97334657-97334903 | Common:3; Rare:93 | ||||
| chr10:97426044-97426397 | Common:2; Rare:154 | ||||
| chr10:97445975-97446252 | Rare:73 | ||||
| chr10:97453369-97453566 | Rare:46 | ||||
| chr10:97455500-97455678 | Rare:46 | ||||
| chr10:97498314-97498555 | Common:2; Rare:107 | ||||
| chr10:97498694-97499057 | Common:2; Rare:106 | ||||
| chr10:97633410-97633596 | Common:2; Rare:46 | ||||
| chr10:97687145-97687546 | Common:6; Rare:118 | ||||
| chr10:98134552-98134695 | Common:1; Rare:46 | ||||
| chr10:98425662-98425869 | Common:1; Rare:55; Clinvar (benign):1; Clinvar (pathogenic):1 |