Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:61901562-61901707 | Common:1; Rare:35 | ||||
chr10:62268601-62268912 | Common:1; Rare:114 | ||||
chr10:63133176-63133383 | Common:2; Rare:66 | ||||
chr10:63269167-63269327 | Common:2; Rare:36 | ||||
chr10:67885109-67885203 | Rare:39 | ||||
chr10:68075196-68075469 | Common:4; Rare:117 | ||||
chr10:68231547-68231640 | Rare:28; Clinvar (pathogenic):1 | ||||
chr10:68331632-68331725 | Rare:19 | ||||
chr10:68331880-68332124 | Common:2; Rare:100 | ||||
chr10:68407252-68407442 | Common:4; Rare:60 | ||||
chr10:68471887-68472033 | Common:1; Rare:77; Clinvar (benign):1 | ||||
chr10:68721090-68721259 | Common:1; Rare:52 | ||||
chr10:68901049-68901352 | Common:3; Rare:120 | ||||
chr10:68956070-68956231 | Rare:64 | ||||
chr10:68988574-68988826 | Common:1; Rare:64; Clinvar (benign):2 |