Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41812760-41813029 | Rare:66; Clinvar:4 | ||||
chr17:41930497-41930665 | Rare:48 | ||||
chr17:41966588-41966831 | Common:1; Rare:83 | ||||
chr17:42017122-42017482 | Rare:113 | ||||
chr17:42154934-42155187 | Common:3; Rare:64 | ||||
chr17:42423093-42423399 | Common:1; Rare:81; Clinvar:2 | ||||
chr17:42458738-42458948 | Common:3; Rare:80 | ||||
chr17:42577671-42577864 | Common:1; Rare:96 | ||||
chr17:42609321-42609732 | Common:8; Rare:173; Clinvar (benign):2 | ||||
chr17:42659365-42659421 | Rare:16 | ||||
chr17:42761027-42761275 | Rare:71 | ||||
chr17:42773375-42773475 | Rare:30 | ||||
chr17:42798643-42798785 | Rare:46 | ||||
chr17:42833333-42833479 | Rare:55 | ||||
chr17:42964428-42964536 | Rare:50 |