chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121601642616016427TC19GENIChomozygous50076243
121601656816016569TC20GENIChomozygous50076245
121601719916017207TGTGTGTG--------19GENIChomozygous50076248
121602025516020256TC22GENIChomozygous50076250
121602028316020284AC19GENIChomozygous50076252
121602028716020288CT20GENIChomozygous50076254
121602097416020975AT21GENIChomozygous50076256
121602118216021183GA19GENIChomozygous50076258
121602128616021287TG23GENIChomozygous50076260
121602233616022337AC23GENIChomozygous50076262
121602308516023086AG24GENIChomozygous50076264
121602328816023289TC15GENIChomozygous50076266
121602329716023298TC14GENIChomozygous50076268
121602331016023311GA13GENIChomozygous50076270
121602348616023487AT4GENIChomozygous50076272
121602356416023565TTTTGG10GENIChomozygous50076274
121602368016023681CT20GENIChomozygous50076276
121602373316023734AG22GENIChomozygous50076278
121602400616024007TC20GENIChomozygous50076280
121602414616024147CT35GENIChomozygous50076282
121602442316024424AG27GENIChomozygous50076284
121602457316024574CT25GENIChomozygous50076286
121602511816025119AG18GENIChomozygous50076288
121602526616025267AG6GENIChomozygous50076290
121602535916025360AT7GENIChomozygous50076292
121602601516026016TC18INTERGENIChomozygous50076294
121602690916026916TTTTTTT-------2INTERGENIChomozygous50282210
121602795116027952G-10INTERGENIChomozygous50076296
121602820116028202CT25INTERGENIChomozygous50076298
121602836916028370CT16INTERGENIChomozygous50076300