Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:98930185-98930447 | Common:1; Rare:72 | ||||
chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:110308524-110308622 | Common:1; Rare:15 | ||||
chr13:111122174-111122305 | Common:1; Rare:29 | ||||
chr14:23415382-23415834 | Common:1; Rare:140; Clinvar:23; Clinvar (benign):14; Clinvar (pathogenic):5 | ||||
chr14:41605331-41605630 | Common:2; Rare:63 | ||||
chr14:49633956-49634087 | Common:1; Rare:57; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862645-49863036 | Common:1; Rare:181 | ||||
chr14:75981846-75982097 | Common:2; Rare:59 | ||||
chr14:81170407-81170489 | Rare:20 | ||||
chr14:81219344-81219504 | Rare:35 | ||||
chr14:85530921-85531131 | Common:1; Rare:37 | ||||
chr14:95516616-95516771 | Common:2; Rare:35 | ||||
chr14:100824271-100824474 | Common:2; Rare:52 | ||||
chr14:100825035-100825307 | Common:1; Rare:53 |