chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103803475938034760TG26GENIChomozygous116563952
103803483838034839AC28GENIChomozygous116760877
103803500438035005CA30GENIChomozygous116563954
103803659238036593TC38GENIChomozygous116869362
103803670838036709GA32GENIChomozygous116563958
103803674538036746CA26GENIChomozygous116563960
103803692738036928AT28GENIChomozygous116563962
103803692838036929GA29GENIChomozygous116563964
103803759938037600CT24GENIChomozygous116869364
103803770838037709GA28GENIChomozygous116869366
103804001838040019CT18GENIChomozygous116869368
103804017338040174TC22GENIChomozygous116563982
103804022438040225GT32GENIChomozygous116869370
103804064238040643CT42GENIChomozygous116760895
103804086238040863AG41GENIChomozygous116563988
103804089338040894AT33GENIChomozygous116563992
103804098438040985AT42GENIChomozygous116869372
103804190538041906CT44GENIChomozygous116869374
103804195738041958TC29GENIChomozygous116563994
103804208938042090TC25GENIChomozygous116563996
103804218138042182GA25GENIChomozygous116563998
103804222838042229TC30GENIChomozygous116564000
103804260438042605GA23GENIChomozygous116869376
103804375138043752TC40GENIChomozygous116564002
103804444038044441TC41GENIChomozygous116564004
103804484038044841AT28GENIChomozygous116564006
103804484138044842AC28GENIChomozygous116564008
103804544338045444AT17GENIChomozygous116564010
103804630238046303TC41GENIChomozygous116564012
103804787738047878TC39GENIChomozygous116869378
103804790838047909GA50GENIChomozygous116869380
103804887938048880AG20GENIChomozygous116564016
103804940438049405TC32GENIChomozygous116564020
103805015838050159TC19GENIChomozygous116564024
103805117838051179TC39GENIChomozygous116564026
103805261538052616TG26GENIChomozygous116564030
103805321938053220TC39GENIChomozygous116564032