chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108850130088501301GT36GENIChomozygous116673886
108850170688501707TC35GENIChomozygous116673888
108850224588502246CT39GENIChomozygous116673890
108850432288504323TC38GENIChomozygous116673892
108850633488506335AG40GENIChomozygous116673894
108850635888506359GC31GENIChomozygous116673896
108850865888508659CG5GENIChomozygous117173708
108850871788508718AG18GENIChomozygous116819067
108850880188508802GA34GENIChomozygous116673898
108851075888510759TC30GENIChomozygous116673900
108851179988511800CT37GENIChomozygous116819069
108851260288512603AG38GENIChomozygous116673902
108851285088512851GA33GENIChomozygous116673904
108851451988514520AT32GENIChomozygous116673906
108851513488515135CT29GENIChomozygous116673908
108851639388516394AT13GENIChomozygous116673910
108851746088517461GA51GENIChomozygous116673912
108851792388517924CT31GENIChomozygous116673914
108851930988519310CA26GENIChomozygous116673922
108851957388519574AG32GENIChomozygous116673924
108851957688519577AG32GENIChomozygous116673926
108851992288519923GA33GENICpossibly homozygous116673928
108852086688520867CT31GENIChomozygous116673930
108852155888521559AG36GENIChomozygous116673932
108852157588521576AG32GENIChomozygous116673934
108852224588522246AT25GENIChomozygous116673936
108852233288522333CT26GENIChomozygous116673938
108852731988527320CT28GENIChomozygous116673940
108852840188528402CG36GENIChomozygous117068379
108852880788528808CT29GENIChomozygous116673942
108852895488528955AG27GENIChomozygous116673944
108853079288530793AT18GENIChomozygous116673946
108853369588533696TG19GENIChomozygous116673954
108853293588532936GT19GENIChomozygous116673948
108853300888533009AG25GENIChomozygous116673950
108853353088533531GA13GENIChomozygous116673952
108853369688533697TC19GENIChomozygous116673956