| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7787971-7788213 | Common:1; Rare:95 | ||||
| chr10:12195790-12196241 | Rare:122 | ||||
| chr10:27155227-27155390 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:31319031-31319226 | Common:2; Rare:61 | ||||
| chr10:32958160-32958493 | Common:2; Rare:130 | ||||
| chr10:45000775-45000951 | Common:1; Rare:73 | ||||
| chr10:45727116-45727280 | Common:3; Rare:57 | ||||
| chr10:45972387-45972554 | Rare:53 | ||||
| chr10:50067804-50067971 | Common:4; Rare:70 | ||||
| chr10:68900994-68901357 | Common:3; Rare:145 | ||||
| chr10:72273671-72273926 | Rare:61 | ||||
| chr10:73167988-73168125 | Rare:27 | ||||
| chr10:73252594-73252783 | Rare:51; Clinvar:4 | ||||
| chr10:97426074-97426302 | Common:2; Rare:99 | ||||
| chr10:97445983-97446242 | Rare:65 |