Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48048069-48048384 | Rare:80 | ||||
chr17:48048628-48048813 | Common:3; Rare:25 | ||||
chr17:48100989-48101110 | Rare:30 | ||||
chr17:48101369-48101614 | Common:2; Rare:75 | ||||
chr17:48590239-48590428 | Common:1; Rare:42 | ||||
chr17:48944773-48944894 | Common:1; Rare:40 | ||||
chr17:48997130-48997477 | Rare:65 | ||||
chr17:49708152-49708379 | Common:1; Rare:72 | ||||
chr17:49788462-49788724 | Common:1; Rare:84 | ||||
chr17:50186315-50186853 | Common:2; Rare:146; Clinvar:16; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:50195449-50195596 | Rare:31; Clinvar (benign):2 | ||||
chr17:50345926-50346136 | Common:4; Rare:69 | ||||
chr17:50373151-50373259 | Common:3; Rare:49 | ||||
chr17:50707592-50707822 | Common:4; Rare:73 | ||||
chr17:50719444-50719652 | Common:1; Rare:82 |