chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139656157139656158GA20GENIChomozygous115937134
7139656331139656332CT11GENIChomozygous115937135
7139657403139657404TG20GENIChomozygous115937136
7139658125139658126TG9GENIChomozygous115937138
7139658343139658344TG12GENIChomozygous115937139
7139658412139658413AG14GENIChomozygous115937140
7139662596139662597AC32GENIChomozygous115937142
7139662690139662691AC29GENIChomozygous115937143
7139664289139664290AG14GENIChomozygous115937144
7139664443139664444GA15GENIChomozygous115937145
7139665621139665622AG26GENIChomozygous115937146
7139666825139666826AG15GENIChomozygous115937147
7139668011139668012GA19GENIChomozygous115937148
7139669539139669540TC21GENIChomozygous115937151
7139669606139669607TC22GENIChomozygous115937152
7139670351139670352GT18GENIChomozygous115937153
7139671307139671308TG29GENIChomozygous115937154
7139676071139676072CA18GENIChomozygous115937155
7139682053139682054TG20GENIChomozygous115937156
7139682941139682942TA25GENIChomozygous115937157
7139683976139683977CT17GENIChomozygous115937158
7139684260139684261TA6GENIChomozygous115937159