| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:49539007-49539227 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941908-49942097 | Rare:57 | ||||
| chr10:50067817-50068008 | Common:5; Rare:85 | ||||
| chr10:50623876-50624084 | Common:1; Rare:82 | ||||
| chr10:50990727-50990938 | Common:3; Rare:35 | ||||
| chr10:50991249-50991610 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chr10:51074137-51074723 | Common:4; Rare:143; Clinvar (benign):9 | ||||
| chr10:51699536-51699641 | Common:1; Rare:42 | ||||
| chr10:58268943-58269254 | Common:5; Rare:96 | ||||
| chr10:58385196-58385492 | Common:4; Rare:93 | ||||
| chr10:59176447-59176658 | Common:4; Rare:71 | ||||
| chr10:60300531-60300787 | Common:1; Rare:44 | ||||
| chr10:63465963-63466137 | Rare:82 | ||||
| chr10:63521190-63521489 | Common:7; Rare:106 | ||||
| chr10:63521789-63521947 | Common:4; Rare:60 |