chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121601642616016427TC17GENIChomozygous50076243
121601656816016569TC16GENIChomozygous50076245
121601719916017207TGTGTGTG--------12GENIChomozygous50076248
121602025516020256TC15GENIChomozygous50076250
121602028316020284AC15GENIChomozygous50076252
121602028716020288CT14GENIChomozygous50076254
121602097416020975AT24GENIChomozygous50076256
121602118216021183GA15GENIChomozygous50076258
121602128616021287TG28GENIChomozygous50076260
121602233616022337AC21GENIChomozygous50076262
121602308516023086AG23GENIChomozygous50076264
121602328816023289TC6GENIChomozygous50076266
121602329716023298TC7GENIChomozygous50076268
121602331016023311GA8GENIChomozygous50076270
121602348616023487AT6GENIChomozygous50076272
121602356416023565TTTTGG14GENIChomozygous50076274
121602368016023681CT7GENIChomozygous50076276
121602373316023734AG11GENIChomozygous50076278
121602400616024007TC14GENIChomozygous50076280
121602414616024147CT25GENIChomozygous50076282
121602442316024424AG27GENIChomozygous50076284
121602511816025119AG20GENIChomozygous50076288
121602526616025267AG12GENIChomozygous50076290
121602535916025360AT5GENIChomozygous50076292
121602601516026016TC31INTERGENIChomozygous50076294
121602820116028202CT11INTERGENIChomozygous50076298
121602836916028370CT11INTERGENIChomozygous50076300
121602691016026917TTTTTTT-------7INTERGENICheterozygous50534205
121602690916026917TTTTTTTT--------7INTERGENICheterozygous50534203