Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110428306-110428584 | Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
chr13:110482306-110482659 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr13:110503852-110504264 | Common:4; Rare:136; Clinvar:1; Clinvar (benign):4 | ||||
chr14:32203246-32203667 | Common:13; Rare:185 | ||||
chr14:32428241-32428417 | Rare:29 | ||||
chr14:34874125-34874231 | Common:1; Rare:30 | ||||
chr14:41605283-41605377 | Common:3; Rare:17 | ||||
chr14:49633956-49634059 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862626-49862999 | Common:1; Rare:170 | ||||
chr14:49868149-49868351 | Common:1; Rare:36 | ||||
chr14:52001530-52001864 | Common:1; Rare:73 | ||||
chr14:52315362-52315633 | Rare:55 | ||||
chr14:74503217-74503522 | Common:2; Rare:109; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:75258927-75259114 | Common:2; Rare:55 | ||||
chr14:75277071-75277287 | Rare:50 |