chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143043069143043070GGT2GENIChomozygous62162470
1143044171143044198GTATATTCTAAATACTACGTGAGCACT---------------------------2GENIChomozygous62727413
1143044397143044398GA5GENIChomozygous61531536
1143045125143045126T-8GENIChomozygous60877228
1143046827143046828CCTTTCTTTTTTTTTTTTTTTTTTTTTTTT1GENIChomozygous62162472
1143048041143048042AG8GENIChomozygous60877229
1143048933143048934A-5GENIChomozygous62724618
1143049366143049367AG8GENIChomozygous62724619
1143050594143050595CCT7GENICheterozygous62328847
1143050618143050619GT9GENIChomozygous60877231
1143053122143053123AG10GENIChomozygous61674515
1143053170143053171TG12GENIChomozygous60877239
1143053250143053251AC3GENIChomozygous61674516
1143053812143053813CA3GENIChomozygous60877241
1143053818143053819A-3GENIChomozygous60877242
1143055605143055606CCAA5GENICheterozygous62162474
1143056168143056169GT8GENIChomozygous62724620
1143056502143056503C-7GENIChomozygous62724621
1143056815143056816CCTT11GENIChomozygous61674519
1143057030143057031TC10GENIChomozygous60877243