chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206343620206343621TA10GENIChomozygous61066628
1206343886206343887GC9GENIChomozygous61066629
1206344033206344034GA8GENIChomozygous61066630
1206345046206345047AG8GENIChomozygous61066631
1206345105206345106AT11GENIChomozygous61066632
1206345374206345375AG7GENIChomozygous61066633
1206346538206346539AC17GENIChomozygous61066634
1206348476206348477TA16GENIChomozygous61066636
1206348956206348957TC15GENIChomozygous62030884
1206350130206350131AG10GENIChomozygous61066637
1206351958206351959AG17GENIChomozygous61066638
1206352232206352233T-18GENICheterozygous61318396
1206352626206352627T-16GENIChomozygous61066639
1206352702206352703TA15GENIChomozygous61066640
1206352823206352824GA12GENIChomozygous61066641
1206352895206352896CCA9GENIChomozygous61066642
1206353067206353068TA10GENIChomozygous61066643
1206353642206353643C-12GENICpossibly homozygous61066644
1206353671206353672TC11GENIChomozygous62030885