chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1183733982183733983TC29INTERGENIChomozygous62027223
1183734456183734457CT30INTERGENIChomozygous62027224
1183734480183734481CT31INTERGENIChomozygous62027225
1183734655183734656A-6INTERGENICheterozygous60997256
1183735106183735107A-17INTERGENIChomozygous61566528
1183736135183736136CT26INTERGENIChomozygous62027227
1183736573183736574AG35INTERGENIChomozygous62027228
1183736771183736772AG40INTERGENIChomozygous62027229
1183737738183737739CT24INTERGENIChomozygous62027230
1183738164183738165CG29INTERGENIChomozygous62027231
1183739582183739583AG27INTERGENIChomozygous62027232
1183739765183739766GA22INTERGENIChomozygous62027233
1183741393183741394AG15INTERGENIChomozygous62027234
1183742030183742031GA22INTERGENIChomozygous62027235
1183742759183742760TC32INTERGENIChomozygous61566533
1183743262183743264TG--17INTERGENICpossibly homozygous61679723
1183743419183743420T-11INTERGENIChomozygous61566534
1183744204183744205AG19INTERGENIChomozygous61566535
1183744448183744449CT32INTERGENIChomozygous62027236