chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134235384042353841CT42GENIChomozygous143578403
134235447042354472AA38GENICpossibly homozygous144924565
134235452142354522TC43GENIChomozygous143578405
134235483942354840CT44GENIChomozygous143578406
134235561642355617AG35GENIChomozygous143578407
134235589542355896AG32GENIChomozygous143578408
134235720442357205GA36GENIChomozygous144929029
134235615442356155GA37GENIChomozygous144929025
134235666042356661GA31GENIChomozygous144929026
134235684542356846GA43GENIChomozygous144929027
134235699942357000GC47GENIChomozygous144929028
134235735442357355TC25GENIChomozygous144929033
134235722442357225CT35GENIChomozygous144929030
134235731542357316CT26GENIChomozygous144929031
134235732942357330TC28GENIChomozygous144929032
134235760742357608CA24GENIChomozygous144929034
134235776542357766GA36GENIChomozygous144929035
134235777642357777AG37GENIChomozygous144929036
134235779542357796AG38GENIChomozygous144929037
134235783142357832GA32GENIChomozygous144929038
134235812342358124TC35GENIChomozygous144929039
134235824342358244CT50GENIChomozygous144929040
134235833642358337TC49GENIChomozygous144929041
134235840342358404GA44GENIChomozygous144929042