chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121601642616016427TC8GENICpossibly homozygous50076243
121601656816016569TC21GENICpossibly homozygous50076245
121602025516020256TC23GENIChomozygous50076250
121602028316020284AC15GENIChomozygous50076252
121602028716020288CT13GENIChomozygous50076254
121602097416020975AT24GENICpossibly homozygous50076256
121602118216021183GA10GENICpossibly homozygous50076258
121602128616021287TG22GENIChomozygous50076260
121602233616022337AC13GENICheterozygous50076262
121602308516023086AG11GENICpossibly homozygous50076264
121602328816023289TC4GENICheterozygous50076266
121602329716023298TC1GENIChomozygous50076268
121602331016023311GA8GENIChomozygous50076270
121602368016023681CT12GENIChomozygous50076276
121602373316023734AG11GENIChomozygous50076278
121602400616024007TC11GENIChomozygous50076280
121602414616024147CT9GENIChomozygous50076282
121602442316024424AG14GENIChomozygous50076284
121602511816025119AG9GENIChomozygous50076288
121602526616025267AG7GENIChomozygous50076290
121602601516026016TC11INTERGENICheterozygous50076294
121602820116028202CT5INTERGENIChomozygous50076298
121602690916026917TTTTTTTT--------1INTERGENIChomozygous50534203