chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103803475938034760TG24GENIChomozygous116563952
103803500438035005CA17GENIChomozygous116563954
103803670838036709GA19GENIChomozygous116563958
103803674538036746CA30GENIChomozygous116563960
103803692738036928AT20GENIChomozygous116563962
103803692838036929GA21GENIChomozygous116563964
103803743938037440CT23GENIChomozygous116563970
103803659238036593TC15GENIChomozygous116869362
103803759938037600CT27GENIChomozygous116869364
103803770838037709GA25GENIChomozygous116869366
103804064238040643CT13GENIChomozygous116760895
103804001838040019CT21GENIChomozygous116869368
103804017338040174TC25GENIChomozygous116563982
103804022438040225GT30GENIChomozygous116869370
103804086238040863AG7GENIChomozygous116563988
103804089338040894AT13GENIChomozygous116563992
103804098438040985AT22GENIChomozygous116869372
103804190538041906CT20GENIChomozygous116869374
103804195738041958TC8GENIChomozygous116563994
103804208938042090TC27GENIChomozygous116563996
103804218138042182GA32GENIChomozygous116563998
103804222838042229TC21GENIChomozygous116564000
103804260438042605GA18GENIChomozygous116869376
103804375138043752TC20GENIChomozygous116564002
103804444038044441TC7GENIChomozygous116564004
103804484038044841AT12GENIChomozygous116564006
103804484138044842AC12GENIChomozygous116564008
103804544338045444AT31GENIChomozygous116564010
103804630238046303TC26GENIChomozygous116564012
103804787738047878TC20GENIChomozygous116869378
103804790838047909GA24GENIChomozygous116869380
103804887938048880AG39GENIChomozygous116564016
103804940438049405TC29GENIChomozygous116564020
103805015838050159TC15GENIChomozygous116564024
103805117838051179TC22GENIChomozygous116564026
103805261538052616TG15GENIChomozygous116564030
103805321938053220TC18GENIChomozygous116564032