chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121601642616016427TC27GENIChomozygous50076243
121601656816016569TC29GENICpossibly homozygous50076245
121601719916017207TGTGTGTG--------18GENICpossibly homozygous50076248
121601720316017207TGTG----18GENICheterozygous50822865
121602025516020256TC26GENIChomozygous50076250
121602028316020284AC24GENIChomozygous50076252
121602028716020288CT24GENIChomozygous50076254
121602097416020975AT21GENIChomozygous50076256
121602118216021183GA20GENIChomozygous50076258
121602128616021287TG16GENIChomozygous50076260
121602233616022337AC9GENIChomozygous50076262
121602308516023086AG28GENICpossibly homozygous50076264
121602328816023289TC17GENIChomozygous50076266
121602329716023298TC17GENIChomozygous50076268
121602331016023311GA17GENIChomozygous50076270
121602347416023478TGTT----10GENICheterozygous50534201
121602348616023487AT8GENICpossibly homozygous50076272
121602356416023565TTTTGG21GENICpossibly homozygous50076274
121602368016023681CT16GENIChomozygous50076276
121602373316023734AG18GENIChomozygous50076278
121602400616024007TC27GENIChomozygous50076280
121602414616024147CT25GENIChomozygous50076282
121602442316024424AG22GENIChomozygous50076284
121602511816025119AG23GENIChomozygous50076288
121602526616025267AG11GENIChomozygous50076290
121602535916025360AT2GENIChomozygous50076292
121602601516026016TC36INTERGENIChomozygous50076294
121602690916026917TTTTTTTT--------15INTERGENICheterozygous50534203
121602691016026917TTTTTTT-------15INTERGENICheterozygous50534205
121602691116026917TTTTTT------15INTERGENICheterozygous50614153
121602820116028202CT15INTERGENIChomozygous50076298
121602836916028370CT13INTERGENIChomozygous50076300
121602841116028412T-19INTERGENICheterozygous50822867