chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266483552266483553CT8GENICpossibly homozygous931251685
1266486512266486513CT9GENIChomozygous931251686
1266486751266486752GA4GENIChomozygous931251687
1266486995266486996CT7GENIChomozygous931251688
1266487893266487894CT9GENIChomozygous931251689
1266488317266488318AG7GENIChomozygous931251690
1266488453266488454TG8GENIChomozygous931251691
1266488457266488458CG8GENIChomozygous931251692
1266488584266488585TC5GENIChomozygous931251693
1266490497266490498CT7GENIChomozygous931251694
1266491321266491322CT4GENIChomozygous931251695
1266491378266491379GA3GENIChomozygous931251696
1266491881266491882GA16GENIChomozygous931251697
1266492131266492132TA8GENIChomozygous931251698
1266492936266492937CT5GENIChomozygous931251699
1266492999266493000GA8GENIChomozygous931251700
1266493001266493002GT9GENIChomozygous931251701
1266493020266493021CT8GENIChomozygous931251702
1266493113266493114CT9GENIChomozygous931251703
1266493239266493240GA10GENIChomozygous931251704
1266494063266494064GA16GENIChomozygous931251705
1266494693266494694AG10GENIChomozygous931251706
1266495790266495791GA14GENIChomozygous931251707
1266496035266496036GA12GENIChomozygous931251708
1266496133266496134TA11GENIChomozygous931251709
1266496146266496147CG6GENIChomozygous931251710
1266496267266496268TC9GENIChomozygous931251711
1266497384266497385AG18GENIChomozygous931251712
1266497641266497642TG17GENIChomozygous931251713
1266497715266497716AG12GENIChomozygous931251714
1266497812266497813CT10GENIChomozygous931251715
1266501507266501508GA6GENIChomozygous931251716
1266506405266506406CT13GENIChomozygous931251717
1266507858266507859TC6GENIChomozygous931251718
1266510619266510620TC10GENIChomozygous931251719