Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:77589729-77589772 | Common:1; Rare:11 | ||||
chr10:86755718-86755877 | Rare:34 | ||||
chr10:86955691-86955785 | Rare:18 | ||||
chr10:86970191-86970519 | Common:5; Rare:117 | ||||
chr10:86971161-86971498 | Common:2; Rare:108 | ||||
chr10:87342273-87342427 | Common:3; Rare:52 | ||||
chr10:88939491-88939863 | Common:1; Rare:70; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr10:88939875-88940002 | Common:1; Rare:14 | ||||
chr10:88943661-88944004 | Common:4; Rare:92; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr10:88948787-88949258 | Rare:89; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88950347-88950378 | Common:1; Rare:5 | ||||
chr10:88951736-88951978 | Rare:34 | ||||
chr10:95332950-95333223 | Common:4; Rare:43 | ||||
chr10:95337277-95337388 | Rare:16 | ||||
chr10:95347319-95347704 | Common:2; Rare:54 |