| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93702450-93702772 | Common:5; Rare:115 | ||||
| chr10:93757666-93757971 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:95290857-95291175 | Common:2; Rare:125 | ||||
| chr10:95561291-95561605 | Common:4; Rare:90 | ||||
| chr10:95907822-95907950 | Common:3; Rare:38 | ||||
| chr10:96130193-96130516 | Common:1; Rare:113 | ||||
| chr10:97334683-97334903 | Common:2; Rare:86 | ||||
| chr10:97426044-97426299 | Common:2; Rare:111 | ||||
| chr10:97445965-97446229 | Common:1; Rare:73 | ||||
| chr10:97498380-97498550 | Common:2; Rare:70 | ||||
| chr10:97498694-97499011 | Common:2; Rare:89 | ||||
| chr10:98134525-98134688 | Common:1; Rare:59 | ||||
| chr10:98268182-98268449 | Common:3; Rare:69 | ||||
| chr10:98425662-98425952 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:99235677-99235731 | Rare:24 |