chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121599217415992175AC7GENIChomozygous967688709
121599415515994156GA26GENIChomozygous967688710
121599416915994170GA22GENIChomozygous967688711
121599507015995071CT16GENIChomozygous967688712
121599507315995074AG17GENIChomozygous967688713
121599589115995892GT9GENIChomozygous967688714
121600420716004208GT12GENICpossibly homozygous967688715
121600590716005908TC34GENIChomozygous967688716
121600768616007687AC29GENIChomozygous967688717
121600879516008796AG14GENIChomozygous967688718
121600901716009018TC16GENIChomozygous967688719
121600945016009451GA26GENIChomozygous967688720
121600963716009638CT25GENIChomozygous967688721
121601035116010352AC17GENIChomozygous967688722
121601044516010446CT18GENIChomozygous967688723
121601066516010666TC34GENIChomozygous967688724
121601110716011108GA38GENIChomozygous967688725