chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134835600548356006AG20GENIChomozygous114549032
134835604848356049CT14GENIChomozygous114615704
134835641848356419CT18GENIChomozygous114615705
134835687748356878TC18GENIChomozygous114615706
134835715548357156GA23GENIChomozygous114615707
134835737448357375AG19GENIChomozygous114549037
134835775648357757CG12GENICpossibly homozygous114615708
134835789648357897CT20GENIChomozygous114615709
134835789748357898CT20GENIChomozygous114615710
134835972248359723TC26GENIChomozygous114549041
134836014048360141GC23GENIChomozygous114549045
134836025948360260TC20GENIChomozygous114549046
134836034448360345GA34GENIChomozygous114549048
134836036748360368CT36GENIChomozygous114549049
134836039748360398AG33GENICpossibly homozygous114549050
134836042148360422CT27GENIChomozygous114549051
134836042648360427TC28GENIChomozygous114549052
134836052248360523GA13GENIChomozygous114549053
134836055148360552AT11GENIChomozygous114549054
134836058948360590GA17GENIChomozygous114549055
134836062748360628CT19GENIChomozygous114549056
134836063048360631TG20GENIChomozygous114549057
134836098348360984AG26GENIChomozygous114549059
134836111048361111CA31GENIChomozygous114549060
134836111248361113GC30GENIChomozygous114549061
134836113948361140TC28GENIChomozygous114615711
134836115248361153GC25GENIChomozygous114615712
134836117948361180CT22GENIChomozygous114615713
134836144848361449CT31GENIChomozygous114549064
134836146248361463CA29GENIChomozygous114549065
134836150948361510GA34GENIChomozygous114549066
134836151148361512TG33GENIChomozygous114549067
134836161548361616AG15GENIChomozygous114549068
134836221048362211GA25GENIChomozygous114549069
134836222148362222AC21GENIChomozygous114549070
134836222348362224AG21GENIChomozygous114549071
134836222448362225TC21GENIChomozygous114549072
134836224448362245TC18GENIChomozygous114549073
134836266348362664CT29GENIChomozygous114549075
134836282148362822TA27GENIChomozygous114615714
134836433648364337AG25GENIChomozygous114549092