chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99429168994291691GG--21GENIChomozygous52861470
99429169494291695GT21GENIChomozygous52861472
99429252794292528GGT26GENIChomozygous52052722
99429252994292530CA26GENIChomozygous52861474
99429270294292703AG28GENIChomozygous52052724
99429322194293222GA19GENIChomozygous52052726
99429420094294201TC28GENIChomozygous52052730
99429510194295102CT25GENIChomozygous52280434
99429518094295181CCGT4GENICheterozygous52052732
99429531694295317AATG18GENIChomozygous52052740
99429729294297293GGA29GENICpossibly homozygous52052746
99429729294297293GGAA29GENICheterozygous53334870
99429795194297952AG29GENIChomozygous52052748
99429908494299085TG34GENIChomozygous52052750
99429936894299369AG27GENIChomozygous52052752
99429948594299486GT18GENIChomozygous52280435
99429980594299806CT25GENIChomozygous52280437
99429992194299922TC16GENIChomozygous52052754
99429998494299985GA17GENIChomozygous52052756
99430047594300476TTCCCCTCCCCC5GENICheterozygous52915542
99430073294300737TTTCG-----3GENIChomozygous53193896
99432041594320416CT11GENIChomozygous52052760
99432248294322483GGT3GENIChomozygous52915543
99432249194322492G-3GENIChomozygous52052766
99431995794319958T-11GENICpossibly homozygous53114099