| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:63521241-63521548 | Common:6; Rare:111 | ||||
| chr10:63521778-63521942 | Common:4; Rare:61 | ||||
| chr10:67884473-67884662 | Common:3; Rare:74 | ||||
| chr10:68331910-68332152 | Common:1; Rare:103 | ||||
| chr10:68332829-68332966 | Common:1; Rare:40 | ||||
| chr10:68407179-68407341 | Common:4; Rare:48 | ||||
| chr10:68527371-68527574 | Common:2; Rare:65 | ||||
| chr10:68901030-68901361 | Common:3; Rare:128 | ||||
| chr10:68956114-68956309 | Common:2; Rare:76 | ||||
| chr10:68988563-68988830 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr10:69087910-69088214 | Rare:67 | ||||
| chr10:69318571-69318953 | Common:5; Rare:108 | ||||
| chr10:69451314-69451612 | Common:2; Rare:83 | ||||
| chr10:70132756-70132905 | Rare:42 | ||||
| chr10:70233288-70233557 | Common:6; Rare:98; Clinvar (benign):1 |