chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32137396621373967TC13GENIChomozygous111501971
32137407621374076AAAAGGAAGAA12GENIChomozygous127859262
32137434721374348TA17GENIChomozygous111501973
32137534921375350AG18GENIChomozygous111501977
32137567221375673TC11GENIChomozygous111501981
32137588121375882AG23GENIChomozygous111501983
32137623321376234CT16GENIChomozygous111501985
32137635721376358GA20GENIChomozygous111501987
32137656421376575AAGTATAAAGT14GENIChomozygous127859264
32137657721376577TC14GENIChomozygous127859265
32137664121376642TC15GENIChomozygous111501989
32137763121377631ATC6GENIChomozygous127859267
32137811421378114ATC8GENIChomozygous127859268
32137886221378863C20GENIChomozygous132581868
32137936021379361GT8GENIChomozygous111501991
32137997421379977AAT6GENIChomozygous127859269
32138022821380229GA6GENIChomozygous112379114
32138171921381720GA21GENIChomozygous111501997
32138177421381775GC23GENIChomozygous111501999
32138178921381790AT22GENIChomozygous111502001
32138180221381802AAGTGCTAGCAC24GENIChomozygous127859272
32138188121381882TG29GENIChomozygous111502003
32138192321381924TA28GENICpossibly homozygous111502005
32137983321379834CA2GENIChomozygous127977115
32138042321380424GA3GENIChomozygous127977116
32138058621380587TC2GENIChomozygous127977118
32138077821380779GA10GENIChomozygous112094531
32138078621380787CT10GENIChomozygous112094532
32138110221381103CT23GENICheterozygous112094533