chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109074113109074114TC11GENIChomozygous70528418
6109110538109110539AC19GENIChomozygous70528456
6109110607109110608CA11GENIChomozygous70528460
6109110609109110610G11GENICheterozygous72163858
6109110695109110696GT4GENIChomozygous70528486
6109111777109111778GC15GENIChomozygous70528506
6109132927109132928CT11GENIChomozygous70528551
6109133425109133426TC11GENIChomozygous70528558
6109133508109133509TA10GENIChomozygous71675885
6109141644109141645CT21INTERGENIChomozygous71675887
6109110640109110641A6GENIChomozygous72929029
6109145317109145318CT4INTERGENIChomozygous72929030
6109148401109148402GA16INTERGENIChomozygous71675889
6109150691109150692AG18INTERGENIChomozygous71675891
6109151376109151377AG18INTERGENIChomozygous70528665
6109152968109152969TC9INTERGENIChomozygous70528669
6109154007109154008GA13INTERGENIChomozygous71675893
6109154773109154774CT10INTERGENIChomozygous70528673
6109165879109165880GT12GENICheterozygous70528707
6109167483109167484GC5GENIChomozygous70528727
6109172360109172361C14GENIChomozygous72163870
6109176348109176349GA21GENIChomozygous71675895
6109177981109177982CA6GENIChomozygous71833398
6109179687109179688AG16GENIChomozygous70528755
6109181198109181198T25INTERGENICheterozygous72929031