chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1183733982183733983TC17INTERGENIChomozygous62027223
1183734456183734457CT14INTERGENIChomozygous62027224
1183734480183734481CT16INTERGENICpossibly homozygous62027225
1183735106183735107A-4INTERGENICheterozygous61566528
1183736135183736136CT15INTERGENIChomozygous62027227
1183736573183736574AG26INTERGENIChomozygous62027228
1183736771183736772AG23INTERGENICpossibly homozygous62027229
1183737738183737739CT28INTERGENIChomozygous62027230
1183738164183738165CG10INTERGENICpossibly homozygous62027231
1183739582183739583AG18INTERGENIChomozygous62027232
1183739765183739766GA8INTERGENIChomozygous62027233
1183741393183741394AG17INTERGENIChomozygous62027234
1183742030183742031GA13INTERGENICpossibly homozygous62027235
1183742759183742760TC17INTERGENIChomozygous61566533
1183743419183743420T-5INTERGENIChomozygous61566534
1183744204183744205AG25INTERGENICpossibly homozygous61566535
1183744448183744449CT26INTERGENICpossibly homozygous62027236