chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410385924103860TA16GENIChomozygous959131073
142410427124104272TC18GENIChomozygous959131074
142410436724104368TC26GENIChomozygous959131075
142410441624104417GC14GENIChomozygous959131076
142410471824104719GA19GENIChomozygous959131077
142410474224104743TC23GENIChomozygous959131078
142410961424109615TC10GENIChomozygous959131079
142410964224109643CT7GENIChomozygous959131080
142410982324109824GT20GENIChomozygous959131081
142410989424109895GT22GENIChomozygous959131082
142410999024109991GC22GENIChomozygous959131083
142411653724116538TC22GENIChomozygous959131084
142411671024116711GA26GENIChomozygous959131085
142411704524117046AC28GENIChomozygous959131086
142411943824119439TA21GENIChomozygous959131087
142411988824119889GA17GENIChomozygous959131088
142412123724121238GA9GENIChomozygous959131089
142412148724121488GA22GENIChomozygous959131090
142412186924121870AT23GENIChomozygous959131091
142412329224123293GT17GENIChomozygous959131092
142412331324123314GC24GENICpossibly homozygous959131093
142412389124123892GC23GENIChomozygous959131094
142412524224125243TC36GENIChomozygous959131095