chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1255564837255564843ACACAC------2GENIChomozygous61167208
1255566191255566192GA10GENIChomozygous61167209
1255567226255567227AG10GENIChomozygous61167211
1255568573255568574TA17GENICpossibly homozygous61167213
1255568685255568686GA17GENIChomozygous62305038
1255566559255566560AG17GENICpossibly homozygous62305035
1255567702255567703CT16GENICpossibly homozygous62305036
1255567773255567774TA15GENICpossibly homozygous62305037
1255568947255568948TTGCCTTGGA2GENICheterozygous62305039
1255569019255569020A-14GENIChomozygous62305040
1255569987255569988AG24GENIChomozygous62305041
1255570603255570604CT18GENICpossibly homozygous62305042
1255570998255570999GA31GENICheterozygous62305043
1255570999255571000AG31GENICheterozygous61167219
1255571824255571825GA20GENIChomozygous62305044
1255572103255572104CT19GENIChomozygous62305045
1255572461255572462TC12GENICpossibly homozygous62305046
1255572776255572777A-1GENIChomozygous62276996
1255572900255572901T-5GENIChomozygous62305047
1255573218255573219AAACAACATACAAC2GENIChomozygous62305048
1255573674255573675GA10GENICpossibly homozygous62305049
1255575092255575093GC15GENIChomozygous62305050
1255575147255575148CT26GENIChomozygous61167229
1255575627255575628CT15GENIChomozygous62305051
1255575796255575797AG21GENICpossibly homozygous62305052
1255576165255576166CA18GENIChomozygous62305053
1255576251255576252CCATT1GENIChomozygous62305054
1255576405255576406AAACCCAGTCCAAATG2GENIChomozygous62305055
1255576410255576411AG3GENIChomozygous62305056
1255576490255576491CCAATCAA5GENICheterozygous62305057
1255576648255576649GT14GENIChomozygous62305058
1255643589255643590T-2INTERGENICheterozygous61167267