chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2173904540173904541AG18GENIChomozygous59223014
2173905709173905710GA27GENIChomozygous59223016
2173906463173906464CCT8GENICheterozygous59223018
2173907171173907172AAG16GENIChomozygous59223020
2173907355173907356GA16GENIChomozygous59223022
2173908108173908109T-6GENIChomozygous59223024
2173909145173909146AAAG22GENIChomozygous59223026
2173911489173911490A-28GENICheterozygous59901315
2173912804173912805GGCACACA18GENICpossibly homozygous59223028
2173912804173912805GGCA18GENICheterozygous59223030
2173914025173914026TA14GENIChomozygous59223032
2173915727173915728TTA22GENIChomozygous59223034
2173917069173917070CT21GENIChomozygous59223036
2173918080173918081CG22GENIChomozygous59223038
2173918869173918870GA27GENIChomozygous59223040
2173919719173919720GA19GENIChomozygous59223042
2173920283173920284CCATGT3GENIChomozygous59223044
2173920635173920636T-8GENIChomozygous59223046
2173921572173921573AAC15GENICheterozygous59223048
2173921957173921958TC28GENIChomozygous59223050
2173922061173922062TC18GENIChomozygous59223051
2173923209173923210AG21GENIChomozygous59223053
2173924101173924103AA--11GENIChomozygous59223055
2173925201173925205TGTG----11GENICheterozygous59223057
2173925203173925205TG--11GENICpossibly homozygous59764641