chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109095809090958091AAG10GENIChomozygous715106322
109096044090960441CT25GENIChomozygous576665205
109096331090963311GC14GENIChomozygous604000996
109096337490963375GC11GENIChomozygous576665206
109096401290964016AAAA----11GENIChomozygous715106323
109096401590964016AAGTG6GENIChomozygous715106324
109096401790964018AT11GENIChomozygous604000997
109096406290964063TG9GENIChomozygous576665207
109096501390965014CCTGTGTG11GENICheterozygous715106328
109096501390965014CCTGTGTGTG11GENICheterozygous715106329
109096509290965093GA15GENIChomozygous604000998
109096514990965150TC10GENIChomozygous576665208
109096523690965240TTGT----14GENIChomozygous715106330
109096557790965578TTCA14GENIChomozygous715106331
109096561690965617TTACACACACACACACACACAC8GENIChomozygous715106334
109096636590966366GGT14GENICpossibly homozygous715106336
109096643190966432CCT3GENIChomozygous715106337
109096699790966998A-9GENIChomozygous715106340
109096778790967788GA19GENIChomozygous576665209
109096788790967888TC9GENIChomozygous604000999
109096795190967952TG17GENIChomozygous576665210
109096807790968078AG24GENIChomozygous576665211