| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27155270-27155391 | Common:3; Rare:41; Clinvar (benign):3 | ||||
| chr10:31319048-31319226 | Common:2; Rare:51 | ||||
| chr10:42782684-42782811 | Rare:30 | ||||
| chr10:45000775-45000953 | Common:1; Rare:74 | ||||
| chr10:45972387-45972541 | Rare:45 | ||||
| chr10:49941929-49942091 | Rare:44 | ||||
| chr10:52314073-52314297 | Common:1; Rare:54 | ||||
| chr10:68721064-68721242 | Common:1; Rare:56 | ||||
| chr10:73252565-73252783 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:73495613-73495759 | Rare:27 | ||||
| chr10:73744256-73744424 | Common:1; Rare:45 | ||||
| chr10:73781915-73782078 | Common:1; Rare:52 | ||||
| chr10:75210480-75210834 | Rare:110 | ||||
| chr10:76318720-76319062 | Common:3; Rare:64 | ||||
| chr10:87094912-87095206 | Common:1; Rare:67; Clinvar:2 |