Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:21994183-21994469 | Rare:105; Clinvar:16; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
chr9:21994586-21995074 | Common:3; Rare:113 | ||||
chr9:26892332-26892478 | Rare:65 | ||||
chr9:33025093-33025339 | Common:6; Rare:105 | ||||
chr9:33264706-33265120 | Rare:115 | ||||
chr9:34329236-34329588 | Rare:103 | ||||
chr9:34637715-34638134 | Common:3; Rare:109 | ||||
chr9:34652015-34652211 | Rare:55 | ||||
chr9:35658016-35658355 | Common:6; Rare:233; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):29 | ||||
chr9:35689712-35690058 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr9:35732108-35732361 | Common:1; Rare:78 | ||||
chr9:35732365-35732723 | Common:3; Rare:89 | ||||
chr9:35814998-35815081 | Rare:26 | ||||
chr9:35815088-35815275 | Rare:37 | ||||
chr9:37800707-37800899 | Common:1; Rare:66 |