chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116448800164488002GGGAA12GENIChomozygous50802188
116448844464488445AG13GENIChomozygous50802190
116448867864488679GA11GENIChomozygous50802193
116448890464488905AG13GENIChomozygous50802195
116448996764489968CT17GENIChomozygous50802197
116449024564490246GT16GENIChomozygous50802199
116449027364490274TC22GENIChomozygous50802201
116449258164492582CT23GENIChomozygous50802206
116449268164492683AG--19GENIChomozygous50802207
116449366664493667GA9GENIChomozygous50802219
116449458464494585AAT17GENIChomozygous50802221
116449548364495484AG20GENIChomozygous50802223
116449663164496632A-18GENIChomozygous50802227
116449672764496728TC21GENIChomozygous50802229
116449674264496768CACACACACACACACACACACACACA--------------------------16GENIChomozygous50802231
116449676864496769CT5GENIChomozygous51186666
116449709664497097GA17GENIChomozygous50802233
116449815864498159AG20GENIChomozygous50802243
116449893764498939AA--22GENICpossibly homozygous50802247
116449894164498943AA--23GENICpossibly homozygous50802249
116449903464499035GA20GENIChomozygous50802251
116449918164499182GC13GENIChomozygous50802253
116449921564499216CT13GENIChomozygous50802255
116450520764505208TC14INTERGENIChomozygous50802257
116450521464505215TC11INTERGENIChomozygous50802259