chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56057436360574364AG18GENIChomozygous113825083
56057479660574797TC12GENIChomozygous113825085
56057493360574934CT19GENIChomozygous113825087
56057585260575853TC18GENIChomozygous113825089
56057605060576051CT27GENIChomozygous113825091
56057642860576429GA27GENIChomozygous113825093
56057666760576668GA12GENIChomozygous113825095
56057673760576738CT10GENIChomozygous113825097
56057676860576769CT7GENICheterozygous113825099
56057753760577538TC15GENIChomozygous113825113
56057850960578510GC14GENIChomozygous113825115
56057860060578601CT4GENIChomozygous113825117
56057875860578759TC5GENIChomozygous113825119
56057956860579569AG19GENICheterozygous113825121
56057989960579900AG13GENIChomozygous113825123
56058028660580287CT10GENIChomozygous113825125
56058056260580563TC10GENIChomozygous113825127
56058153060581531CT9GENIChomozygous113825133
56058171560581716AG10GENIChomozygous113825139
56058176260581763GA13GENIChomozygous113825141
56058254660582547TC14GENIChomozygous113825143
56058342360583424TC9GENIChomozygous113825145
56058363360583634TC10GENIChomozygous113825147
56058423360584234TA10GENIChomozygous113825149
56058438560584386AT15GENIChomozygous113825151
56058567360585674CT20GENIChomozygous113825155
56058584860585849AG28GENIChomozygous113825157
56058592960585930GA10GENIChomozygous113825159
56058616560586166AC10GENIChomozygous113825161
56058755560587556CT8GENIChomozygous113825163
56058799860587999GA11GENIChomozygous113825165