Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27100409-27100582 | Common:3; Rare:52; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155203-27155390 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
chr10:27240466-27240628 | Common:1; Rare:53 | ||||
chr10:27240715-27240910 | Rare:51 | ||||
chr10:27242058-27242211 | Common:1; Rare:66 | ||||
chr10:28532715-28532862 | Common:1; Rare:58 | ||||
chr10:28533076-28533200 | Rare:51 | ||||
chr10:28677317-28677521 | Common:2; Rare:93 | ||||
chr10:29634930-29635108 | Rare:34 | ||||
chr10:30059503-30059678 | Common:1; Rare:65 | ||||
chr10:30433834-30434221 | Common:4; Rare:112 | ||||
chr10:30434540-30434708 | Common:1; Rare:47 | ||||
chr10:31031841-31032052 | Common:2; Rare:85 | ||||
chr10:31032382-31032619 | Common:10; Rare:76 |