| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95290829-95291175 | Common:2; Rare:134 | ||||
| chr10:95656604-95656888 | Common:1; Rare:82; Clinvar:6; Clinvar (benign):2 | ||||
| chr10:95693695-95694209 | Common:6; Rare:171; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr10:95907679-95907927 | Common:2; Rare:67 | ||||
| chr10:96043425-96043584 | Common:1; Rare:60 | ||||
| chr10:96129942-96130090 | Common:1; Rare:56 | ||||
| chr10:96586458-96586650 | Common:2; Rare:60 | ||||
| chr10:96586749-96586825 | Common:2; Rare:30 | ||||
| chr10:96586844-96587252 | Common:4; Rare:165 | ||||
| chr10:96831958-96832299 | Common:1; Rare:132 | ||||
| chr10:97334670-97334876 | Common:3; Rare:81 | ||||
| chr10:97426023-97426256 | Common:3; Rare:90 | ||||
| chr10:97445969-97446237 | Common:1; Rare:71 | ||||
| chr10:97460906-97461202 | Common:2; Rare:69 | ||||
| chr10:97498350-97498563 | Common:2; Rare:91 |