Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110308500-110308547 | Common:1; Rare:13 | ||||
chr13:110424731-110425009 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110438375-110438650 | Common:7; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr13:110449511-110449786 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
chr13:110503853-110504264 | Common:4; Rare:135; Clinvar:1; Clinvar (benign):3 | ||||
chr13:113129386-113129466 | Common:1; Rare:27 | ||||
chr14:21069549-21069644 | Common:1; Rare:22 | ||||
chr14:22845145-22845295 | Rare:53 | ||||
chr14:23416937-23417198 | Common:3; Rare:83; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
chr14:41605282-41605453 | Common:4; Rare:38 | ||||
chr14:49633956-49634061 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49789554-49789604 | Rare:13 | ||||
chr14:49862642-49863039 | Common:1; Rare:182 | ||||
chr14:51599902-51600029 | Rare:31 | ||||
chr14:51600032-51600219 | Rare:27 |