chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32299922422999225CG54GENIChomozygous111505802
32300074223000743TG61GENIChomozygous111505803
32300118323001184CG70GENIChomozygous111505804
32300141323001414AG73GENICpossibly homozygous111505805
32300164023001641AG49GENIChomozygous111505806
32300164823001649AG48GENIChomozygous111505807
32300234723002348CT60GENIChomozygous111505808
32300236123002362TA54GENIChomozygous111505809
32300236223002363TA52GENIChomozygous111505810
32300247923002480CA70GENIChomozygous111505811
32300318423003185GA61GENIChomozygous111505812
32300353723003538TC41GENIChomozygous111505813
32300413523004136GA56GENICpossibly homozygous111505814
32300601223006013AG59GENIChomozygous111505815
32300773623007737CT74GENICpossibly homozygous111505816
32300812723008128CT53GENIChomozygous111505817
32300832923008330CT55GENIChomozygous111505818
32300839723008398AG68GENIChomozygous111505819
32300859923008600CT67GENIChomozygous111505820
32300872823008729AG49GENIChomozygous111505821
32300889123008892CT39GENIChomozygous111505822
32300908623009087CG47GENIChomozygous111505823
32300926523009266TC60GENIChomozygous111505824
32300927123009272CT61GENIChomozygous111505825
32301093223010933TC53GENIChomozygous111505826
32301100923011010TC55GENICpossibly homozygous111505827
32301116323011164CT62GENICpossibly homozygous111505828
32301202723012028GA69GENIChomozygous111505829
32301307123013072GC54GENIChomozygous111505830
32301336123013362CT41GENICpossibly homozygous111505831
32301336723013368TC49GENICheterozygous111505832
32301337323013374TC47GENICheterozygous111505833
32301349423013495AG51GENIChomozygous111505836
32301358623013587GC55GENICpossibly homozygous111505837
32301697423016975TC48GENIChomozygous111505838
32301866423018665TC84GENICpossibly homozygous111505839