Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71819516-71819801 | Common:1; Rare:113; Clinvar:4; Clinvar (benign):2 | ||||
chr10:72273639-72273942 | Rare:77 | ||||
chr10:72354904-72355196 | Common:2; Rare:105 | ||||
chr10:72626038-72626310 | Common:1; Rare:66 | ||||
chr10:73167970-73168142 | Rare:42 | ||||
chr10:73252594-73252791 | Rare:53; Clinvar:4 | ||||
chr10:73625962-73626093 | Rare:24 | ||||
chr10:73744257-73744422 | Common:1; Rare:43 | ||||
chr10:73874506-73874738 | Rare:56 | ||||
chr10:74151042-74151235 | Common:1; Rare:50 | ||||
chr10:74176631-74176790 | Rare:45; Clinvar:2 | ||||
chr10:75210473-75210611 | Rare:36 | ||||
chr10:78029494-78029637 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chr10:80078614-80078696 | Rare:30 | ||||
chr10:80079082-80079286 | Common:2; Rare:85 |