Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:125091731-125091892 | Common:2; Rare:55; Clinvar (benign):2 | ||||
chr8:143018423-143018491 | Rare:19 | ||||
chr9:4679447-4679669 | Rare:101 | ||||
chr9:20684037-20684269 | Common:4; Rare:92 | ||||
chr9:33025125-33025304 | Common:4; Rare:75 | ||||
chr9:34329269-34329615 | Common:1; Rare:97 | ||||
chr9:35657986-35658386 | Common:6; Rare:288; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
chr9:35689840-35690287 | Common:4; Rare:128; Clinvar:3; Clinvar (benign):1 | ||||
chr9:35732100-35732334 | Common:1; Rare:67 | ||||
chr9:35732373-35732676 | Common:2; Rare:76 | ||||
chr9:37422613-37422730 | Common:2; Rare:61 | ||||
chr9:75088200-75088536 | Common:3; Rare:121 | ||||
chr9:83707942-83708236 | Common:2; Rare:82 | ||||
chr9:83980178-83980406 | Rare:89 | ||||
chr9:83980556-83980761 | Common:3; Rare:89 |