Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:85582262-85582389 | Rare:33 | ||||
chr1:85582571-85582952 | Common:1; Rare:116 | ||||
chr1:117366596-117366866 | Common:1; Rare:78 | ||||
chr1:155904456-155904737 | Common:2; Rare:80; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:156676625-156676790 | Rare:49 | ||||
chr1:210233770-210234038 | Common:8; Rare:92 | ||||
chr1:220880025-220880125 | Rare:32 | ||||
chr1:230867912-230868069 | Common:1; Rare:38 | ||||
chr1:240093133-240093449 | Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr10:22437921-22438211 | Common:6; Rare:49 | ||||
chr10:70164360-70164415 | Rare:8 | ||||
chr10:73247247-73247414 | Rare:93 | ||||
chr10:73730456-73730603 | Common:1; Rare:37 | ||||
chr10:74070732-74071078 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):7 | ||||
chr10:79826342-79826398 | Common:1; Rare:17 |