chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47761518277615183GA27GENIChomozygous112736296
47761566077615661TG40GENIChomozygous112736298
47761709877617099TC37GENIChomozygous112736300
47761723377617234CA28GENIChomozygous112736302
47761785777617858TG23GENIChomozygous112736304
47761799677617997TA31GENIChomozygous112736306
47761831977618320CT17GENIChomozygous112736308
47761862677618627AC27GENICheterozygous113276696
47761876277618763TG20GENIChomozygous112736310
47761930277619303CA27GENIChomozygous112736312
47761950977619510CT29GENIChomozygous112736314
47761968377619684CT31GENIChomozygous112736316
47762008577620086AG34GENIChomozygous112736318
47762035077620351GC29GENIChomozygous112736320
47762062077620621GA36GENIChomozygous112736322
47762068977620690CT33GENIChomozygous112736324
47761858477618585AT9GENICpossibly homozygous113124365
47761858577618586CG9GENICpossibly homozygous113124367
47762408077624081CT51GENIChomozygous112736326
47762470577624706CT38GENIChomozygous112736328
47762493577624936GA40GENIChomozygous112736330
47762630177626302AG42GENIChomozygous112736332
47762757177627572GA39GENIChomozygous112736334
47762884877628849TA28GENIChomozygous112736336
47762897377628974TG29GENIChomozygous112736338
47763011677630117CG32GENIChomozygous112736340
47763051777630518CT26GENIChomozygous112736342
47763072877630729TC38GENIChomozygous112736344
47763089477630895TC39GENIChomozygous112736346
47763154477631545CT28GENIChomozygous112736348
47763164477631645AG39GENIChomozygous112736350
47763170877631709CA35GENIChomozygous112736352
47763236577632366GA22GENIChomozygous112736354
47763348277633483CT26GENIChomozygous112736356
47763357177633572AC32GENIChomozygous112736358
47763373177633732GA31GENIChomozygous112736360
47763447777634478CA41GENIChomozygous112736362
47763449477634495TC37GENIChomozygous112736364
47763453877634539GA37GENIChomozygous112736366
47763477477634775CA40GENIChomozygous112736368