chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124933065649330657TC18GENIChomozygous115348885
124933080249330803TC11GENIChomozygous115348887
124933109949331100AC8GENIChomozygous115348891
124933124249331243TC11GENIChomozygous115348893
124933167249331673GA24GENIChomozygous115401044
124933535049335351TG26GENIChomozygous115348907
124933649749336498TC8GENIChomozygous115348909
124933680349336804GA19GENIChomozygous115401048
124933685249336853AG15GENIChomozygous115348913
124933813749338138GT11GENIChomozygous115348917
124933869449338695CT12GENIChomozygous123651123
124933944649339447CG14GENIChomozygous115348921
124934322649343227GT6GENICheterozygous126246020
124934556349345564CT12GENIChomozygous123651127
124934672549346726CG22GENIChomozygous123651129
124935412649354127CT26GENIChomozygous123651130
124935504549355046TC14GENIChomozygous115401066
124936098649360987CT6GENIChomozygous123651136
124936318749363188CT22GENIChomozygous123651137
124936786949367870CT21GENIChomozygous123651139
124936930149369302AG3GENICheterozygous126246021
124937301749373018AG16GENIChomozygous115348933
124937654149376542AG18GENIChomozygous115348935
124937775249377753AG4GENIChomozygous115401118
124938154249381543AC4GENICheterozygous115521758