chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130241657130241658CT14GENICpossibly homozygous54110679
7130242161130242162AG13GENICpossibly homozygous54110680
7130242204130242205GT17GENIChomozygous54110681
7130242219130242220AT11GENIChomozygous54110682
7130242230130242231AG12GENIChomozygous54110683
7130242556130242557TC20GENICpossibly homozygous54110684
7130243328130243329CT14GENIChomozygous54110686
7130244010130244011GA24GENIChomozygous54110689
7130244149130244150TC16GENIChomozygous54110690
7130244239130244240GT15GENICpossibly homozygous54110691
7130244339130244340TC19GENIChomozygous54110692
7130244569130244571CA--2GENIChomozygous54754847
7130244646130244647TC9GENICpossibly homozygous54110693
7130244968130244969TA25GENICpossibly homozygous54754849
7130245237130245238TTGA18GENICheterozygous54110697
7130245454130245455AG25GENIChomozygous54110698
7130245485130245486CA7GENICpossibly homozygous54110699
7130246022130246023AG10GENICpossibly homozygous54110700
7130246569130246570CT15GENICpossibly homozygous54754851
7130246638130246639AG16GENICpossibly homozygous54110702
7130246825130246826GT4GENIChomozygous54754853
7130246832130246833AT4GENIChomozygous54754855
7130247163130247164TC3GENIChomozygous54110705
7130247273130247274CT17GENIChomozygous54110706
7130247462130247463TC16GENIChomozygous54110707
7130247942130247943CT11GENIChomozygous54754857
7130248118130248119TG22GENICpossibly homozygous54521253
7130249323130249324GC17GENICpossibly homozygous54110709
7130249386130249387AC15GENIChomozygous54521261
7130249478130249480CC--8GENIChomozygous54521263
7130249481130249487TCCTAC------9GENIChomozygous54521265
7130249685130249686GC17GENICpossibly homozygous54110710
7130249847130249848AT17GENICpossibly homozygous54110711
7130250109130250110TC3GENIChomozygous54110713