Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:50623876-50624079 | Common:1; Rare:80 | ||||
chr10:51074402-51074626 | Common:1; Rare:52; Clinvar (benign):5 | ||||
chr10:56361232-56361475 | Common:5; Rare:77 | ||||
chr10:58268959-58269231 | Common:5; Rare:80 | ||||
chr10:62049221-62049459 | Rare:55 | ||||
chr10:63269061-63269388 | Common:2; Rare:63 | ||||
chr10:63465965-63466053 | Rare:42 | ||||
chr10:68331926-68332111 | Common:1; Rare:81 | ||||
chr10:68332884-68332911 | Rare:6 | ||||
chr10:68407214-68407356 | Common:4; Rare:43 | ||||
chr10:69087932-69088172 | Rare:48 | ||||
chr10:70170458-70170681 | Common:3; Rare:76 | ||||
chr10:71773466-71773693 | Common:3; Rare:74 | ||||
chr10:72273917-72273942 | Rare:14 | ||||
chr10:73096804-73097024 | Common:3; Rare:68 |