chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125182735125182736GA17GENIChomozygous108214982
1125183055125183056AG17GENIChomozygous108214986
1125183064125183065TC16GENIChomozygous108214987
1125184485125184486GA29GENIChomozygous108214989
1125185566125185567GA27GENIChomozygous108214991
1125185571125185572GA27GENIChomozygous108214992
1125185678125185679TC24GENIChomozygous108214993
1125185732125185733GC29GENIChomozygous108214994
1125185734125185735AG32GENIChomozygous108214995
1125185740125185741TC30GENIChomozygous108214996
1125186598125186599CT22GENIChomozygous108214997
1125187177125187178GA13GENIChomozygous108214999
1125187223125187224GC18GENIChomozygous108215000
1125187759125187760AC24GENIChomozygous108215001
1125188509125188510AG21GENIChomozygous108215003
1125188549125188550CT26GENIChomozygous108215004
1125189357125189358CT23GENIChomozygous108215005
1125189415125189416TC21GENIChomozygous108215006
1125190143125190144GA29GENIChomozygous108215009
1125190170125190171GT29GENIChomozygous108215010
1125190264125190265GA24GENIChomozygous108215011
1125190268125190269GA22GENIChomozygous108215012
1125190427125190428GC22GENIChomozygous108215013
1125192531125192532AG30GENIChomozygous108215032
1125192622125192623TC15GENIChomozygous108924959
1125192903125192904CT30GENIChomozygous109134127
1125193261125193262AG33GENIChomozygous108215033
1125193846125193847AG30GENIChomozygous108215038
1125194518125194519TC28GENIChomozygous108215044
1125197383125197384GC14GENIChomozygous108924962
1125198291125198292AG31GENIChomozygous108215057
1125200294125200295GA21GENIChomozygous108215068
1125203268125203269TC37GENIChomozygous108215087
1125197855125197856GA20GENIChomozygous120568193
1125206616125206617AG18GENIChomozygous108215119
1125208820125208821CG26GENIChomozygous120568197
1125209720125209721CG9GENIChomozygous120568199