chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143040601143040602AG18GENIChomozygous61674500
1143041427143041428C-16GENIChomozygous61674501
1143042514143042547GTCGTCGTCGTCGTCGTCGTCGTCGTCTTCTTC---------------------------------3GENICheterozygous62162468
1143043069143043070GGT3GENICheterozygous62162470
1143044194143044195CT23GENIChomozygous60877226
1143044197143044198TA23GENIChomozygous60877227
1143044369143044370CCA13GENICheterozygous61674508
1143044397143044398GA17GENIChomozygous61531536
1143045125143045126T-24GENIChomozygous60877228
1143046827143046828CCTTTCTTTTTTTTTTTTTTTTTTTTTTTT2GENIChomozygous62162472
1143048041143048042AG20GENIChomozygous60877229
1143048683143048684TTA26GENIChomozygous61674510
1143049324143049325GT27GENIChomozygous61674511
1143050618143050619GT15GENIChomozygous60877231
1143053170143053171TG32GENIChomozygous60877239
1143053250143053251AC40GENIChomozygous61674516
1143053812143053813CA10GENIChomozygous60877241
1143053818143053819A-10GENIChomozygous60877242
1143056815143056816CCTT34GENIChomozygous61674519
1143057030143057031TC29GENIChomozygous60877243
1143057845143057846GA24GENICpossibly homozygous61674521
1143050823143050824GGAGAGAC1GENIChomozygous62246598
1143053245143053246TC43GENIChomozygous61902629