| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:91633047-91633381 | Common:2; Rare:99 | ||||
| chr10:91923735-91923821 | Rare:30 | ||||
| chr10:92290935-92291393 | Common:5; Rare:139 | ||||
| chr10:92574008-92574129 | Common:1; Rare:35 | ||||
| chr10:92592952-92593178 | Common:3; Rare:66 | ||||
| chr10:92689737-92689955 | Common:1; Rare:71 | ||||
| chr10:92848344-92848536 | Rare:74 | ||||
| chr10:93482108-93482466 | Common:2; Rare:96 | ||||
| chr10:93496377-93496647 | Common:4; Rare:67 | ||||
| chr10:93566550-93566717 | Common:2; Rare:43 | ||||
| chr10:93893917-93894031 | Rare:50 | ||||
| chr10:95290837-95291186 | Common:2; Rare:136 | ||||
| chr10:95561324-95561611 | Common:4; Rare:88 | ||||
| chr10:95656647-95656908 | Rare:74; Clinvar:5 | ||||
| chr10:95693869-95694192 | Common:5; Rare:107; Clinvar (benign):3; Clinvar (pathogenic):1 |