Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:46818712-46818862 | Rare:26 | ||||
chr17:47323871-47323962 | Rare:33 | ||||
chr17:47941385-47941702 | Rare:86; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:47957822-47958109 | Common:1; Rare:50 | ||||
chr17:48048075-48048446 | Rare:97 | ||||
chr17:48944788-48944869 | Common:1; Rare:21 | ||||
chr17:49210591-49210711 | Rare:19 | ||||
chr17:49994672-49994860 | Rare:56; Clinvar:2 | ||||
chr17:50373151-50373259 | Common:3; Rare:49 | ||||
chr17:50426119-50426257 | Rare:34 | ||||
chr17:50534404-50534622 | Common:1; Rare:54 | ||||
chr17:50719469-50719704 | Rare:95 | ||||
chr17:50866342-50866774 | Common:3; Rare:121 | ||||
chr17:51260137-51260625 | Common:3; Rare:193 | ||||
chr17:51260747-51260776 | Rare:13 |