chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150686278150686279CT12GENIChomozygous114348916
5150687272150687273CT19GENIChomozygous114348918
5150688837150688838TC17GENIChomozygous119021232
5150690664150690665GA23GENIChomozygous114348922
5150690906150690907TC26GENICpossibly homozygous114348924
5150691388150691389CT10GENIChomozygous114348928
5150691430150691431AG18GENIChomozygous114540368
5150692118150692119TA5GENIChomozygous114348932
5150692120150692121GC5GENIChomozygous114348934
5150692122150692123TC6GENIChomozygous114348936
5150692348150692349AG13GENIChomozygous119021234
5150694736150694737TC9GENIChomozygous114540378
5150695760150695761CT26GENIChomozygous114348944
5150696850150696851GA8GENIChomozygous118943809
5150697663150697664GA7GENIChomozygous119021236
5150699962150699963CT19GENIChomozygous119021238
5150700269150700270GA23GENIChomozygous119021240
5150701466150701467TC32GENIChomozygous114348956
5150702419150702420CT20GENIChomozygous119021242
5150703071150703072AC14GENIChomozygous114348958