chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32299922422999225CG16GENIChomozygous111505802
32300118323001184CG38GENIChomozygous111505804
32300141323001414AG28GENIChomozygous111505805
32300164023001641AG24GENIChomozygous111505806
32300164823001649AG23GENIChomozygous111505807
32300234723002348CT35GENIChomozygous111505808
32300236123002362TA34GENIChomozygous111505809
32300236223002363TA34GENIChomozygous111505810
32300247923002480CA27GENIChomozygous111505811
32300318423003185GA21GENIChomozygous111505812
32300353723003538TC22GENIChomozygous111505813
32300413523004136GA27GENIChomozygous111505814
32300601223006013AG26GENIChomozygous111505815
32300773623007737CT23GENIChomozygous111505816
32300812723008128CT45GENICpossibly homozygous111505817
32300832923008330CT35GENIChomozygous111505818
32300839723008398AG30GENIChomozygous111505819
32300859923008600CT28GENIChomozygous111505820
32300872823008729AG26GENIChomozygous111505821
32300889123008892CT26GENIChomozygous111505822
32300908623009087CG25GENIChomozygous111505823
32300926523009266TC22GENIChomozygous111505824
32300927123009272CT26GENIChomozygous111505825
32301093223010933TC35GENIChomozygous111505826
32301100923011010TC33GENIChomozygous111505827
32301116323011164CT29GENIChomozygous111505828
32301202723012028GA38GENIChomozygous111505829
32301307123013072GC26GENICpossibly homozygous111505830
32301349423013495AG25GENIChomozygous111505836
32301358623013587GC27GENIChomozygous111505837
32301697423016975TC29GENIChomozygous111505838
32301866423018665TC29GENIChomozygous111505839