chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121598217515982176TC5GENIChomozygous890358917
121598515415985155GC6GENIChomozygous890358918
121599415515994156GA4GENIChomozygous890358919
121599416915994170GA7GENIChomozygous890358920
121599477215994773GA9GENIChomozygous890358921
121599507015995071CT10GENIChomozygous890358922
121599507315995074AG11GENIChomozygous890358923
121599589115995892GT12GENIChomozygous890358924
121599945515999456GC4GENIChomozygous890358925
121600420716004208GT22GENIChomozygous890358926
121600566816005669GA6GENIChomozygous890358927
121600590716005908TC7GENIChomozygous890358928
121600768616007687AC23GENIChomozygous890358929
121600879516008796AG17GENIChomozygous890358930
121600901716009018TC10GENIChomozygous890358931
121600945016009451GA13GENIChomozygous890358932
121600963716009638CT8GENIChomozygous890358933
121601035116010352AC9GENIChomozygous890358934
121601044516010446CT19GENIChomozygous890358935
121601066516010666TC24GENICpossibly homozygous890358936
121601110716011108GA11GENIChomozygous890358937