chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121601642616016427TC52GENIChomozygous50076243
121601656816016569TC49GENIChomozygous50076245
121601719916017207TGTGTGTG--------12GENIChomozygous50076248
121602025516020256TC61GENIChomozygous50076250
121602028316020284AC62GENIChomozygous50076252
121602028716020288CT62GENIChomozygous50076254
121602097416020975AT45GENICpossibly homozygous50076256
121602118216021183GA51GENIChomozygous50076258
121602128616021287TG58GENIChomozygous50076260
121602233616022337AC47GENIChomozygous50076262
121602308516023086AG62GENIChomozygous50076264
121602328816023289TC51GENIChomozygous50076266
121602329716023298TC55GENIChomozygous50076268
121602331016023311GA47GENIChomozygous50076270
121602347116023472AC17GENICheterozygous50282209
121602348616023487AT8GENIChomozygous50076272
121602356416023565TTTTGG11GENIChomozygous50076274
121602368016023681CT50GENIChomozygous50076276
121602373316023734AG54GENIChomozygous50076278
121602400616024007TC57GENICpossibly homozygous50076280
121602414616024147CT59GENIChomozygous50076282
121602442316024424AG45GENIChomozygous50076284
121602457316024574CT49GENIChomozygous50076286
121602511816025119AG54GENIChomozygous50076288
121602526616025267AG52GENIChomozygous50076290
121602535916025360AT47GENIChomozygous50076292
121602601516026016TC61INTERGENIChomozygous50076294
121602690916026916TTTTTTT-------2INTERGENIChomozygous50282210
121602795116027952G-31INTERGENIChomozygous50076296
121602820116028202CT42INTERGENIChomozygous50076298
121602836916028370CT56INTERGENIChomozygous50076300