| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95290490-95290774 | Common:1; Rare:61 | ||||
| chr10:95290809-95291291 | Common:3; Rare:173 | ||||
| chr10:95561357-95561621 | Common:4; Rare:82 | ||||
| chr10:95656543-95657005 | Common:1; Rare:121; Clinvar:6; Clinvar (benign):4 | ||||
| chr10:95693782-95694061 | Common:2; Rare:105; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95755468-95755752 | Common:1; Rare:48 | ||||
| chr10:95756012-95756195 | Common:1; Rare:47 | ||||
| chr10:95756456-95756626 | Common:1; Rare:42 | ||||
| chr10:95838634-95838868 | Common:1; Rare:48 | ||||
| chr10:95907395-95907531 | Common:1; Rare:29 | ||||
| chr10:95907794-95907982 | Common:3; Rare:62 | ||||
| chr10:96043278-96043638 | Common:2; Rare:122 | ||||
| chr10:96129689-96129828 | Rare:29 | ||||
| chr10:96129882-96130406 | Common:4; Rare:184 | ||||
| chr10:96130411-96130749 | Common:1; Rare:104 |