chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174739762047397621CA23GENIChomozygous111057317
174740075947400760AG21GENIChomozygous111057318
174740090647400907TC19GENIChomozygous111057319
174740317347403174TA16GENIChomozygous111057320
174740377047403771GC31GENIChomozygous111057321
174740383347403834AG27GENIChomozygous111057322
174740491347404914GC21GENIChomozygous111057323
174740579947405800TC16GENIChomozygous111057324
174740697247406973CT23GENIChomozygous111057325
174740803147408032CT22GENIChomozygous111057326
174740858547408586CT18GENIChomozygous111057327
174740911447409115TC26GENICpossibly homozygous111057328
174740921847409219CT25GENIChomozygous111057329
174740583547405836T19GENIChomozygous129454217
174740600547406005CTGTAGTC14GENIChomozygous129454218
174740964447409644AAAG17GENIChomozygous129454219
174741092747410933TCCTCT9GENICpossibly homozygous129454220
174741133747411338A19GENIChomozygous129454221
174741648447416485AC24GENIChomozygous111057338
174741050747410508AG21GENIChomozygous111057330
174741104347411044TC20GENIChomozygous111057331
174741120547411206TC15GENIChomozygous111057332
174741266147412662AT20GENIChomozygous111057333
174741367647413677CT16GENIChomozygous111057334
174741374247413743TC18GENIChomozygous111057335
174741559647415597AT19GENIChomozygous111057336
174741596247415963GA19GENIChomozygous111057337
174741091447410915CT6GENIChomozygous119342902
174741694947416950GT19GENICpossibly homozygous111057339
174741727747417278AG21GENIChomozygous111057340
174741814247418143TG15GENIChomozygous111057341
174741890047418901TG22GENIChomozygous111057342
174741893847418939TA18GENIChomozygous111057343
174741939447419395GT20GENIChomozygous111057344
174741977847419779CT23GENIChomozygous111057345
174742001847420019T19GENIChomozygous129454222
174742022447420225CG32GENIChomozygous111057346
174742188147421883TT16GENIChomozygous129454223
174741089847410899CT9GENIChomozygous129497413