Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70146616-70146927 | Common:1; Rare:82 | ||||
chr10:70170414-70170676 | Common:4; Rare:88 | ||||
chr10:70233323-70233563 | Common:6; Rare:86; Clinvar (benign):1 | ||||
chr10:70403983-70404179 | Rare:73 | ||||
chr10:70815789-70816103 | Rare:106 | ||||
chr10:70885796-70886023 | Rare:62; Clinvar:1 | ||||
chr10:70888229-70888318 | Rare:22 | ||||
chr10:70888520-70888695 | Common:2; Rare:58; Clinvar:5; Clinvar (benign):2 | ||||
chr10:71773490-71773751 | Common:3; Rare:74 | ||||
chr10:72216227-72216336 | Rare:51 | ||||
chr10:72273699-72274060 | Rare:111 | ||||
chr10:72354779-72355022 | Common:2; Rare:105 | ||||
chr10:73096788-73097028 | Common:3; Rare:75 | ||||
chr10:73097038-73097124 | Common:1; Rare:22 | ||||
chr10:73110363-73110534 | Rare:35 |