chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174739762047397621CA49GENIChomozygous111057317
174740075947400760AG53GENIChomozygous111057318
174740090647400907TC59GENIChomozygous111057319
174740317347403174TA41GENIChomozygous111057320
174740377047403771GC55GENIChomozygous111057321
174740383347403834AG44GENIChomozygous111057322
174740491347404914GC56GENIChomozygous111057323
174740579947405800TC43GENIChomozygous111057324
174740697247406973CT53GENIChomozygous111057325
174740803147408032CT52GENIChomozygous111057326
174740858547408586CT43GENIChomozygous111057327
174740911447409115TC53GENIChomozygous111057328
174740921847409219CT50GENIChomozygous111057329
174741050747410508AG41GENIChomozygous111057330
174741104347411044TC32GENIChomozygous111057331
174741120547411206TC40GENIChomozygous111057332
174741266147412662AT40GENIChomozygous111057333
174741367647413677CT50GENIChomozygous111057334
174741374247413743TC56GENIChomozygous111057335
174741559647415597AT46GENICpossibly homozygous111057336
174741596247415963GA57GENIChomozygous111057337
174741648447416485AC65GENIChomozygous111057338
174741694947416950GT62GENIChomozygous111057339
174741727747417278AG52GENIChomozygous111057340
174741814247418143TG44GENIChomozygous111057341
174741890047418901TG58GENIChomozygous111057342
174741893847418939TA57GENIChomozygous111057343
174741939447419395GT64GENIChomozygous111057344
174741977847419779CT35GENIChomozygous111057345
174742022447420225CG54GENIChomozygous111057346
174740583547405836T40GENIChomozygous129454217
174740600547406005CTGTAGTC46GENIChomozygous129454218
174740964447409644AAAG48GENIChomozygous129454219
174741092747410933TCCTCT18GENIChomozygous129454220
174741133747411338A49GENIChomozygous129454221
174742001847420019T47GENICpossibly homozygous129454222
174742188147421883TT54GENIChomozygous129454223
174741089847410899CT22GENIChomozygous129497413
174741091447410915CT19GENIChomozygous119342902