Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10638843-10639219 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):1 | ||||
chr17:10639275-10639838 | Common:6; Rare:150; Clinvar:2; Clinvar (benign):11 | ||||
chr17:10641084-10641373 | Common:2; Rare:68; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:10645705-10646034 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:10647180-10647427 | Rare:46; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:10656720-10656796 | Common:1; Rare:19 | ||||
chr17:43315658-43315916 | Common:6; Rare:108 | ||||
chr17:50189812-50189913 | Common:2; Rare:22; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:64837117-64837310 | Common:1; Rare:55 | ||||
chr17:64975559-64975716 | Common:1; Rare:54 | ||||
chr17:65100708-65100906 | Rare:59 | ||||
chr17:76557631-76557854 | Common:1; Rare:78 | ||||
chr17:76563121-76563161 | Rare:10 | ||||
chr17:80959454-80959985 | Common:5; Rare:121 | ||||
chr17:80961535-80961793 | Common:3; Rare:47 |