Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40444706-40444814 | Common:1; Rare:15 | ||||
chr17:40456176-40456832 | Common:1; Rare:155; Clinvar (pathogenic):1 | ||||
chr17:40550743-40550881 | Common:2; Rare:12 | ||||
chr17:41503035-41503349 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):5 | ||||
chr17:41503393-41503689 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
chr17:42050588-42050806 | Common:1; Rare:55 | ||||
chr17:42422443-42422523 | Common:1; Rare:18 | ||||
chr17:42422614-42422804 | Rare:81; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:42422813-42422861 | Rare:18 | ||||
chr17:42554297-42554610 | Common:1; Rare:107 | ||||
chr17:42851749-42851896 | Common:1; Rare:67 | ||||
chr17:43002750-43002807 | Common:1; Rare:22 | ||||
chr17:43315628-43315916 | Common:7; Rare:120 | ||||
chr17:43388301-43388428 | Rare:26 | ||||
chr17:43848430-43848742 | Rare:80 |