chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32299892822998936CAGGGCTG37GENIChomozygous127860514
32299922422999225CG48GENIChomozygous111505802
32300074223000743TG49GENIChomozygous111505803
32300118323001184CG53GENIChomozygous111505804
32300141323001414AG50GENIChomozygous111505805
32300164023001641AG70GENIChomozygous111505806
32300164823001649AG66GENIChomozygous111505807
32300234723002348CT69GENIChomozygous111505808
32300236123002362TA68GENIChomozygous111505809
32300236223002363TA67GENIChomozygous111505810
32300247923002480CA62GENIChomozygous111505811
32300259923002599ATCCCTGGGTTATCCATACCACTTTAGCACTGCCATACT44GENIChomozygous127860515
32300318423003185GA56GENIChomozygous111505812
32300353723003538TC51GENIChomozygous111505813
32300413523004136GA37GENIChomozygous111505814
32300601223006013AG47GENIChomozygous111505815
32300773623007737CT54GENIChomozygous111505816
32300812723008128CT55GENIChomozygous111505817
32300832923008330CT50GENIChomozygous111505818
32300839723008398AG39GENIChomozygous111505819
32300859923008600CT62GENIChomozygous111505820
32300872823008729AG41GENIChomozygous111505821
32300886223008862G61GENICpossibly homozygous127860516
32300886523008865CAACTTCTACTAGAGC62GENICpossibly homozygous127860517
32300889123008892CT58GENIChomozygous111505822
32300908623009087CG49GENIChomozygous111505823
32300926523009266TC44GENIChomozygous111505824
32300927123009272CT44GENIChomozygous111505825
32300976823009768GG31GENIChomozygous127860518
32301093223010933TC63GENIChomozygous111505826
32301100923011010TC70GENIChomozygous111505827
32301116323011164CT65GENIChomozygous111505828
32301202723012028GA61GENIChomozygous111505829
32301307123013072GC64GENIChomozygous111505830
32301349423013495AG66GENIChomozygous111505836
32301358623013587GC61GENIChomozygous111505837
32301697423016975TC50GENIChomozygous111505838
32301866423018665TC49GENIChomozygous111505839
32301041323010413GA66GENIChomozygous127860519