chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212727237212727241TTTG----47GENIChomozygous61076601
1212728962212728963GGA20GENIChomozygous61076602
1212729493212729494CCT12GENICheterozygous61076603
1212729890212729891AG44GENICpossibly homozygous61076604
1212731180212731181CCAGAT8GENIChomozygous61076605
1212731849212731850AG29GENIChomozygous61076606
1212732133212732134TA54GENIChomozygous61076607
1212732283212732284TC44GENIChomozygous61076608
1212732898212732899AG74GENIChomozygous61076609
1212732908212732909GA75GENIChomozygous61076610
1212733279212733280AG46GENIChomozygous61076611
1212733415212733416TC52GENIChomozygous61076612
1212733737212733738CCA21GENICpossibly homozygous61076613
1212733767212733768A-20GENICpossibly homozygous61076614
1212733790212733791CA32GENICpossibly homozygous61076615
1212733798212733799AAAC4GENICheterozygous61076616
1212734086212734087CG59GENIChomozygous61076617
1212734571212734572CT52GENIChomozygous61076618
1212734635212734636TC54GENIChomozygous61076619
1212735014212735015TTC48GENIChomozygous61076620
1212735154212735155AG62GENIChomozygous61076621
1212736375212736376GA10GENIChomozygous61076622
1212736375212736376GC15GENIChomozygous61076623
1212736629212736630CT36GENIChomozygous61076624
1212736674212736675AT41GENIChomozygous61076625
1212736689212736690GA46GENIChomozygous61076626
1212737698212737699TC48GENIChomozygous61076627
1212738397212738398TG50GENIChomozygous61076628
1212738749212738750GA26GENIChomozygous61076629