chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73710338537103385TTCTTGGTAAGTCTGTAAGC40GENICpossibly homozygous128453882
73711325737113258TA37GENICheterozygous131877868
73711327637113277TC32GENICheterozygous130669512
73711435737114358GA4GENIChomozygous116143337
73711874937118750CT55GENIChomozygous115647989
73712757037127571A31GENIChomozygous128453883
73713299937133000TC45GENICpossibly homozygous115647990
73714736237147362A45GENIChomozygous128453884
73715235537152356GA40GENIChomozygous115647991
73715239937152399G34GENIChomozygous128453885
73715241137152412GA38GENIChomozygous115647992
73715259037152591CA52GENIChomozygous115647993
73716046737160468TC35GENIChomozygous115647994
73716895937168960TC35GENIChomozygous115647995
73717752637177527CT20GENICheterozygous130767529
73717755437177555TA15GENICheterozygous128550619
73717755737177558TG15GENICheterozygous128550620
73717756937177570GA14GENICheterozygous134705549
73718165537181656AG24GENICheterozygous128550624
73718381237183813CT35GENIChomozygous115648000
73718401537184016GT48GENICheterozygous116402796
73718401637184017CT48GENICheterozygous122758214
73718402037184021GA47GENICheterozygous122758215
73718402137184022CG47GENICheterozygous122758216
73718402737184028CT49GENICheterozygous116402797
73718402837184029AT46GENICheterozygous115648002
73718403837184039GC44GENICheterozygous115648003
73718403937184040GT44GENICheterozygous116021639
73717984737179848C2GENIChomozygous130342387