Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2336430-2336556 | Rare:47 | ||||
chr17:2337270-2337631 | Common:1; Rare:105 | ||||
chr17:2393792-2394106 | Common:3; Rare:120 | ||||
chr17:2400749-2400822 | Rare:14 | ||||
chr17:2401029-2401246 | Rare:65 | ||||
chr17:2511766-2511975 | Common:2; Rare:56 | ||||
chr17:2593091-2593277 | Rare:44 | ||||
chr17:2593437-2593697 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
chr17:2593835-2593998 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
chr17:2776562-2776920 | Common:6; Rare:103 | ||||
chr17:3636241-3636496 | Common:4; Rare:71; Clinvar (benign):1 | ||||
chr17:3636574-3636768 | Common:2; Rare:54; Clinvar:4; Clinvar (benign):2 | ||||
chr17:3668552-3668863 | Common:2; Rare:127 | ||||
chr17:3723752-3723922 | Common:1; Rare:93 | ||||
chr17:3845753-3845887 | Rare:35 |