| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101667929-101668047 | Rare:36; Clinvar:1 | ||||
| chr10:101694426-101694465 | Rare:15 | ||||
| chr10:101694469-101694594 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr10:101812984-101813090 | Rare:22 | ||||
| chr10:102066180-102066292 | Rare:44; Clinvar:1 | ||||
| chr10:102109476-102109671 | Common:1; Rare:47 | ||||
| chr10:102121339-102121610 | Rare:38 | ||||
| chr10:102352239-102352507 | Common:1; Rare:54 | ||||
| chr10:102449796-102449870 | Common:1; Rare:14 | ||||
| chr10:102642778-102642952 | Common:1; Rare:33 | ||||
| chr10:102655986-102656136 | Common:4; Rare:40 | ||||
| chr10:102705422-102705723 | Common:2; Rare:65 | ||||
| chr10:102777073-102777330 | Common:2; Rare:43 | ||||
| chr10:103098973-103099265 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr10:103116634-103116691 | Rare:4 |