Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71819465-71819895 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851183-71851427 | Common:5; Rare:106; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216228-72216318 | Rare:45 | ||||
chr10:72216384-72216505 | Common:2; Rare:20 | ||||
chr10:72273544-72273658 | Rare:27 | ||||
chr10:72273901-72274377 | Common:2; Rare:160 | ||||
chr10:72354882-72355192 | Common:2; Rare:111 | ||||
chr10:72626047-72626302 | Common:1; Rare:62 | ||||
chr10:72691905-72692271 | Common:2; Rare:119 | ||||
chr10:73167925-73168366 | Rare:129 | ||||
chr10:73252552-73252821 | Common:2; Rare:80; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495606-73495784 | Rare:43 | ||||
chr10:73495813-73495849 | Rare:16 | ||||
chr10:73495970-73496024 | Rare:12 | ||||
chr10:73625951-73626128 | Rare:35 |