Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5420127-5420210 | Rare:34 | ||||
chr17:5438887-5439047 | Rare:52 | ||||
chr17:5486157-5486607 | Common:5; Rare:152 | ||||
chr17:5619415-5619618 | Common:3; Rare:49 | ||||
chr17:5772824-5772955 | Common:4; Rare:57 | ||||
chr17:6444199-6444468 | Common:2; Rare:84 | ||||
chr17:6640646-6641097 | Common:7; Rare:141 | ||||
chr17:6651553-6651767 | Common:1; Rare:76 | ||||
chr17:7012323-7012705 | Rare:126 | ||||
chr17:7242285-7242541 | Common:1; Rare:93 | ||||
chr17:7484241-7484371 | Common:1; Rare:53 | ||||
chr17:7583610-7583865 | Common:1; Rare:105; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7857875-7858066 | Rare:64 | ||||
chr17:7931874-7932235 | Common:5; Rare:95 | ||||
chr17:8162931-8163122 | Common:1; Rare:70 |