chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32299892822998936CAGGGCTG37GENIChomozygous127860514
32299922422999225CG47GENIChomozygous111505802
32300074223000743TG75GENIChomozygous111505803
32300118323001184CG51GENIChomozygous111505804
32300141323001414AG63GENIChomozygous111505805
32300164023001641AG68GENIChomozygous111505806
32300164823001649AG67GENIChomozygous111505807
32300234723002348CT54GENICpossibly homozygous111505808
32300236123002362TA56GENIChomozygous111505809
32300236223002363TA56GENIChomozygous111505810
32300247923002480CA53GENIChomozygous111505811
32300259923002599ATCCCTGGGTTATCCATACCACTTTAGCACTGCCATACT49GENIChomozygous127860515
32300318423003185GA40GENIChomozygous111505812
32300353723003538TC48GENIChomozygous111505813
32300413523004136GA24GENIChomozygous111505814
32300601223006013AG39GENIChomozygous111505815
32300773623007737CT53GENIChomozygous111505816
32300812723008128CT56GENIChomozygous111505817
32300832923008330CT46GENIChomozygous111505818
32300839723008398AG44GENIChomozygous111505819
32300859923008600CT67GENIChomozygous111505820
32300872823008729AG60GENIChomozygous111505821
32300886223008862G51GENIChomozygous127860516
32300886523008865CAACTTCTACTAGAGC53GENIChomozygous127860517
32300889123008892CT66GENIChomozygous111505822
32300908623009087CG48GENIChomozygous111505823
32300926523009266TC42GENIChomozygous111505824
32300927123009272CT41GENIChomozygous111505825
32300976823009768GG29GENIChomozygous127860518
32301041323010413GA48GENIChomozygous127860519
32301093223010933TC48GENIChomozygous111505826
32301100923011010TC49GENIChomozygous111505827
32301116323011164CT51GENIChomozygous111505828
32301202723012028GA61GENIChomozygous111505829
32301307123013072GC55GENIChomozygous111505830
32301349423013495AG76GENIChomozygous111505836
32301358623013587GC57GENIChomozygous111505837
32301697423016975TC51GENIChomozygous111505838
32301866423018665TC72GENIChomozygous111505839