| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:94362901-94363027 | Common:2; Rare:51 | ||||
| chr10:94545711-94545796 | Common:2; Rare:26 | ||||
| chr10:95290836-95291186 | Common:2; Rare:136 | ||||
| chr10:95693856-95694067 | Common:2; Rare:84; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95756103-95756214 | Common:2; Rare:40 | ||||
| chr10:95756381-95756591 | Common:1; Rare:47 | ||||
| chr10:96129943-96130063 | Common:1; Rare:48 | ||||
| chr10:96832105-96832304 | Rare:76 | ||||
| chr10:97401217-97401526 | Common:1; Rare:111 | ||||
| chr10:97426032-97426256 | Common:3; Rare:86 | ||||
| chr10:97445975-97446187 | Rare:56 | ||||
| chr10:98446263-98446403 | Rare:23 | ||||
| chr10:98446757-98446838 | Rare:18 | ||||
| chr10:99430616-99430900 | Common:3; Rare:63 | ||||
| chr10:99732069-99732284 | Rare:72; Clinvar:4; Clinvar (benign):1 |