chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
165017971750179718TG14GENIChomozygous112409879
165017974050179741GC4GENIChomozygous112409881
165017997350179974TA15GENIChomozygous112409883
165018001150180012CT13GENIChomozygous112409885
165018003550180036CT12GENIChomozygous112409887
165018008750180088AG4GENIChomozygous111814383
165018014350180144TG12GENIChomozygous111814385
165018040150180402AT17GENIChomozygous111814387
165018099450180995GA19GENIChomozygous112409889
165018106050181061CA11GENIChomozygous112409891
165018116350181164CT8GENIChomozygous112409893
165018137950181380CG14GENIChomozygous112409897
165018150150181502CT18GENIChomozygous112061056
165018161750181618TG21GENIChomozygous112409899
165018280950182810GT13GENIChomozygous112409901
165018488650184887GA8GENIChomozygous111814409
165018494350184944TC10GENIChomozygous112061062
165018520850185209GA20GENIChomozygous112409903
165018598050185981TC19GENIChomozygous111814411
165018749450187495GT12GENIChomozygous112409905
165018775450187755GA11GENIChomozygous112409907
165018790250187903TC19GENIChomozygous112409909
165018793150187932GA13GENIChomozygous112409911
165018818550188186AG13GENIChomozygous111814440
165018896250188963AG12GENIChomozygous111814448
165018906150189062TC23GENIChomozygous111814450
165018909050189091AT13GENIChomozygous111814452
165018918550189186AG12GENIChomozygous112409913
165018922650189227GT12GENIChomozygous112409915
165018927950189280AG14GENIChomozygous112409917
165018941050189411TC17GENIChomozygous112409919
165018950750189508CT16GENIChomozygous112409921
165018954850189549GA21GENIChomozygous111814458
165018959950189600GT17GENIChomozygous112409923
165018967850189679TC18GENIChomozygous112409925
165018782250187823TC16GENIChomozygous111981768
165019061550190616GT14GENIChomozygous125661565