Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659219-99659554 | Common:1; Rare:85 | ||||
chr10:99732070-99732331 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185888-100186096 | Rare:77 | ||||
chr10:100229566-100229664 | Rare:31 | ||||
chr10:100267616-100267733 | Common:2; Rare:38 | ||||
chr10:100286623-100286761 | Common:3; Rare:76 | ||||
chr10:100346911-100347475 | Common:3; Rare:131 | ||||
chr10:100529837-100530010 | Common:1; Rare:44 | ||||
chr10:100912751-100913011 | Common:1; Rare:80 | ||||
chr10:100913328-100913454 | Rare:33 | ||||
chr10:100987194-100987582 | Common:1; Rare:142; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996969-100997132 | Common:1; Rare:44 | ||||
chr10:101031113-101031279 | Common:1; Rare:37 | ||||
chr10:101588195-101588336 | Rare:55 | ||||
chr10:101783357-101783479 | Rare:56 |