| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93702478-93702708 | Common:4; Rare:86 | ||||
| chr10:93893890-93893997 | Common:1; Rare:46 | ||||
| chr10:94362866-94363027 | Common:3; Rare:60 | ||||
| chr10:95290837-95291133 | Common:2; Rare:106 | ||||
| chr10:95415275-95415472 | Common:1; Rare:31 | ||||
| chr10:95561338-95561605 | Common:4; Rare:80 | ||||
| chr10:95693869-95694153 | Common:5; Rare:100; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907865-95908213 | Common:2; Rare:81 | ||||
| chr10:96130228-96130529 | Common:1; Rare:101 | ||||
| chr10:97334694-97334811 | Common:1; Rare:54 | ||||
| chr10:97426047-97426300 | Common:2; Rare:110 | ||||
| chr10:97445983-97446237 | Rare:65 | ||||
| chr10:97498362-97498560 | Common:2; Rare:84 | ||||
| chr10:97498694-97499057 | Common:2; Rare:106 | ||||
| chr10:97633449-97633596 | Common:2; Rare:36 |