chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2195555804195555805GA5GENICheterozygous110195161
2195557310195557311GA7GENIChomozygous120447436
2195562646195562647TC7GENIChomozygous120447438
2195563041195563042AG14GENIChomozygous110195173
2195563720195563721TC10GENIChomozygous110195174
2195563797195563798TC4GENIChomozygous110195176
2195564450195564451CT10GENIChomozygous120378966
2195564862195564863AC16GENIChomozygous120378967
2195565605195565606AT6GENIChomozygous120378968
2195565790195565791GA15GENIChomozygous110195177
2195566041195566042CT19GENIChomozygous120378969
2195566247195566248CA19GENIChomozygous120378970
2195566283195566284TA20GENIChomozygous120378971
2195566633195566634TC9GENIChomozygous120378973
2195566661195566662AG19GENIChomozygous120378974
2195567705195567706TC20GENIChomozygous120378975
2195568229195568230CT21GENIChomozygous120378976
2195568380195568381GA18GENIChomozygous120378977
2195569312195569313CT19GENIChomozygous120378978
2195572392195572393AC14GENIChomozygous110195180
2195572647195572648GA6GENICheterozygous125666605
2195572868195572869CT8GENICheterozygous125746337
2195565903195565904AT7GENIChomozygous125746334
2195570367195570368GA21GENIChomozygous125746335
2195570464195570465CA14GENIChomozygous125746336
2195574141195574142TC7GENIChomozygous110195191
2195575545195575546AG19GENIChomozygous110195195
2195575687195575688TC12GENIChomozygous120378980
2195575792195575793CT17GENIChomozygous125746338
2195576137195576138CT20GENIChomozygous120378981
2195576583195576584TC20GENIChomozygous120378982