chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143040601143040602AG20GENIChomozygous61674500
1143041427143041428C-14GENIChomozygous61674501
1143042302143042303CCCTTT7GENICpossibly homozygous62162462
1143042514143042547GTCGTCGTCGTCGTCGTCGTCGTCGTCTTCTTC---------------------------------1GENIChomozygous62162468
1143043069143043070GGT6GENICheterozygous62162470
1143044194143044195CT22GENIChomozygous60877226
1143044197143044198TA22GENIChomozygous60877227
1143044369143044370CCA24GENICpossibly homozygous61674508
1143044397143044398GA29GENIChomozygous61531536
1143045125143045126T-28GENIChomozygous60877228
1143046827143046828CCTTTCTTTTTTTTTTTTTTTTTTTTTTTT2GENIChomozygous62162472
1143048041143048042AG44GENIChomozygous60877229
1143048683143048684TTA26GENIChomozygous61674510
1143049324143049325GT27GENIChomozygous61674511
1143050594143050595CCT3GENICheterozygous62328847
1143050618143050619GT28GENIChomozygous60877231
1143050823143050824GGAGAC3GENICheterozygous62232595
1143050823143050824GGAGAGAC3GENICheterozygous62246598
1143053170143053171TG28GENIChomozygous60877239
1143053250143053251AC31GENIChomozygous61674516
1143053812143053813CA9GENIChomozygous60877241
1143053818143053819A-11GENIChomozygous60877242
1143055605143055606CCAA3GENICheterozygous62162474
1143056815143056816CCTT15GENIChomozygous61674519
1143057030143057031TC31GENIChomozygous60877243
1143057845143057846GA33GENIChomozygous61674521
1143053245143053246TC32GENIChomozygous61902629