| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:75211479-75211585 | Common:2; Rare:39 | ||||
| chr10:75235260-75235640 | Common:5; Rare:100 | ||||
| chr10:75235633-75235877 | Common:3; Rare:260 | ||||
| chr10:75401368-75401569 | Rare:138 | ||||
| chr10:75401717-75401967 | Common:6; Rare:216 | ||||
| chr10:75402260-75402630 | Common:6; Rare:263 | ||||
| chr10:75431553-75431722 | Common:3; Rare:95 | ||||
| chr10:77637610-77638240 | Common:4; Rare:207; Clinvar:6; Clinvar (benign):1 | ||||
| chr10:77638435-77638573 | Rare:35 | ||||
| chr10:77889417-77889630 | Rare:51 | ||||
| chr10:77926259-77926499 | Rare:113 | ||||
| chr10:77926442-77926980 | Common:7; Rare:336 | ||||
| chr10:77927010-77927310 | Common:5; Rare:147 | ||||
| chr10:78029400-78029735 | Common:4; Rare:204; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr10:78033487-78033992 | Common:7; Rare:390; Clinvar (benign):12 |