Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:46030551-46030721 | Common:1; Rare:59 | ||||
chr10:48605076-48605235 | Common:1; Rare:48 | ||||
chr10:49188316-49188480 | Common:2; Rare:46 | ||||
chr10:49298712-49298926 | Common:2; Rare:39 | ||||
chr10:49299002-49299289 | Rare:40 | ||||
chr10:49539023-49539175 | Common:2; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49941915-49942124 | Rare:64 | ||||
chr10:50067701-50068004 | Common:6; Rare:116 | ||||
chr10:50623881-50624084 | Common:1; Rare:81 | ||||
chr10:50624852-50624974 | Common:1; Rare:47 | ||||
chr10:50739915-50739972 | Rare:12 | ||||
chr10:50990658-50991115 | Common:5; Rare:74 | ||||
chr10:50991295-50991370 | Common:2; Rare:28 | ||||
chr10:51074371-51074562 | Rare:41; Clinvar (benign):2 | ||||
chr10:51699557-51699641 | Common:1; Rare:31 |