chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140839133140839134GT23GENIChomozygous112858094
4140848321140848322GT14GENIChomozygous112858104
4140851241140851242AG16GENIChomozygous113057489
4140851289140851290AC23GENIChomozygous113175895
4140851539140851540TC14GENIChomozygous112858112
4140851540140851541GA14GENIChomozygous113175897
4140854949140854950CT35GENIChomozygous113175899
4140855327140855328TC11GENIChomozygous112858128
4140855522140855523AG10GENIChomozygous113057497
4140855669140855670CA20GENIChomozygous112858130
4140855720140855721CA37GENIChomozygous112858132
4140855976140855977CG9GENIChomozygous112858136
4140856740140856741TC33GENIChomozygous112858140
4140857171140857172AG26GENICpossibly homozygous113175901
4140858330140858331CG17GENIChomozygous112858148
4140865458140865459AG20GENIChomozygous112858156
4140869446140869447GA12GENIChomozygous113175903
4140870118140870119GA22GENIChomozygous113175905
4140870654140870655AG19GENICpossibly homozygous113175907
4140871205140871206AG12GENIChomozygous113175909
4140873341140873342AT16GENIChomozygous112858162
4140873879140873880GA24GENIChomozygous113175911
4140876205140876206GA17GENIChomozygous112858164
4140876462140876463CG16GENIChomozygous112858166
4140877210140877211AC21GENIChomozygous113175913
4140879395140879396CT28GENIChomozygous113175915
4140851523140851524TG24GENICheterozygous113242208
4140870658140870659AG18GENICheterozygous113242209
4140870662140870663AG19GENICheterozygous113242210