chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99429168994291691GG--27GENIChomozygous52861470
99429169494291695GT27GENIChomozygous52861472
99429252794292528GGT26GENIChomozygous52052722
99429252994292530CA26GENIChomozygous52861474
99429270294292703AG22GENIChomozygous52052724
99429322194293222GA33GENIChomozygous52052726
99429420094294201TC29GENICpossibly homozygous52052730
99429510194295102CT22GENIChomozygous52280434
99429518094295181CCGT34GENICheterozygous52052732
99429531694295317AATG27GENIChomozygous52052740
99429729294297293GGA15GENIChomozygous52052746
99429795194297952AG27GENIChomozygous52052748
99429908494299085TG37GENIChomozygous52052750
99429936894299369AG41GENIChomozygous52052752
99429948594299486GT24GENIChomozygous52280435
99429980594299806CT25GENIChomozygous52280437
99429992194299922TC24GENIChomozygous52052754
99429998494299985GA52GENIChomozygous52052756
99430047594300476TTCCCCTCCCCC3GENIChomozygous52915542
99432041594320416CT21GENIChomozygous52052760
99432248294322483GGT6GENIChomozygous52915543
99432249194322492G-6GENIChomozygous52052766