Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10645718-10646031 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:10655185-10655461 | Common:2; Rare:48 | ||||
chr17:16441485-16441504 | Rare:1 | ||||
chr17:20091618-20091755 | Rare:26 | ||||
chr17:41503146-41503428 | Common:2; Rare:85; Clinvar (benign):3 | ||||
chr17:41503664-41503998 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr17:41611429-41611689 | Common:3; Rare:83 | ||||
chr17:43315658-43315916 | Common:6; Rare:108 | ||||
chr17:50189690-50189862 | Common:3; Rare:39; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr17:50189865-50190040 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:63989408-63989698 | Rare:62 | ||||
chr17:64975559-64975748 | Common:2; Rare:75 | ||||
chr17:76557683-76557821 | Rare:50 | ||||
chr17:80959542-80959985 | Common:5; Rare:96 | ||||
chr18:5238006-5238125 | Common:1; Rare:49 |