chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130241615130241616AG10GENIChomozygous54110678
7130241657130241658CT7GENICpossibly homozygous54110679
7130242161130242162AG8GENICpossibly homozygous54110680
7130242204130242205GT10GENIChomozygous54110681
7130242219130242220AT7GENIChomozygous54110682
7130242230130242231AG6GENIChomozygous54110683
7130242556130242557TC10GENICpossibly homozygous54110684
7130242783130242784GA8GENICpossibly homozygous54110685
7130243328130243329CT11GENICpossibly homozygous54110686
7130244010130244011GA17GENIChomozygous54110689
7130244149130244150TC13GENIChomozygous54110690
7130244239130244240GT13GENIChomozygous54110691
7130244339130244340TC22GENICpossibly homozygous54110692
7130244646130244647TC13GENICpossibly homozygous54110693
7130244877130244878G-4GENIChomozygous54110694
7130245012130245014TT--1GENIChomozygous54110695
7130245237130245238TTGA13GENIChomozygous54110697
7130245454130245455AG14GENIChomozygous54110698
7130245485130245486CA5GENIChomozygous54110699
7130246022130246023AG10GENICheterozygous54110700
7130246227130246228GA13GENIChomozygous54110701
7130246638130246639AG16GENICpossibly homozygous54110702
7130246693130246694CT21GENIChomozygous54110703
7130246790130246791GA6GENIChomozygous54110704
7130247163130247164TC2GENIChomozygous54110705
7130247273130247274CT14GENIChomozygous54110706
7130247462130247463TC11GENIChomozygous54110707
7130249323130249324GC12GENIChomozygous54110709
7130249685130249686GC10GENIChomozygous54110710
7130249847130249848AT9GENIChomozygous54110711
7130250088130250089TC1GENIChomozygous54110712
7130250109130250110TC2GENICheterozygous54110713