| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:44990224-44990443 | Rare:64 | ||||
| chr10:45594797-45595031 | Common:3; Rare:145 | ||||
| chr10:45672581-45673055 | Common:2; Rare:242 | ||||
| chr10:45727169-45727318 | Common:2; Rare:123 | ||||
| chr10:45972347-45972504 | Common:2; Rare:85 | ||||
| chr10:46030521-46030758 | Common:2; Rare:137 | ||||
| chr10:48306384-48306731 | Common:4; Rare:237 | ||||
| chr10:49538989-49539168 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr10:49941922-49942074 | Rare:79 | ||||
| chr10:50067852-50067991 | Common:4; Rare:112 | ||||
| chr10:50418315-50418540 | Rare:51 | ||||
| chr10:50623860-50624102 | Common:2; Rare:173 | ||||
| chr10:50624460-50624840 | Common:10; Rare:230 | ||||
| chr10:50624785-50625021 | Common:3; Rare:107 | ||||
| chr10:50625159-50625326 | Common:1; Rare:49 |