chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47761518277615183GA39GENIChomozygous112736296
47761566077615661TG18GENIChomozygous112736298
47761567377615674GA20GENIChomozygous113351210
47761709877617099TC22GENIChomozygous112736300
47761785777617858TG34GENICpossibly homozygous112736304
47761807977618080CT20GENIChomozygous113351212
47761831977618320CT22GENIChomozygous112736308
47762035077620351GC24GENIChomozygous112736320
47762262477622625GA22GENIChomozygous113351214
47762341777623418GA34GENIChomozygous113351216
47762610177626102CT22GENIChomozygous113351218
47762630177626302AG19GENIChomozygous112736332
47762821177628212CT25GENIChomozygous113351220
47762864777628648TC22GENIChomozygous113351222
47762885177628852AT21GENICheterozygous113351224
47762897377628974TG25GENIChomozygous112736338
47763011677630117CG22GENIChomozygous112736340
47763051777630518CT32GENIChomozygous112736342
47763072877630729TC26GENIChomozygous112736344
47763079977630800CT24GENIChomozygous113351226
47763089477630895TC20GENIChomozygous112736346
47763154477631545CT20GENIChomozygous112736348
47763164477631645AG20GENIChomozygous112736350
47763170877631709CA21GENIChomozygous112736352
47763236577632366GA32GENIChomozygous112736354
47763270977632710GA22GENIChomozygous113351228
47763348277633483CT43GENIChomozygous112736356
47763357177633572AC48GENIChomozygous112736358
47763373177633732GA50GENIChomozygous112736360
47763447777634478CA35GENIChomozygous112736362
47763449477634495TC31GENIChomozygous112736364
47763453877634539GA37GENIChomozygous112736366
47763477477634775CA19GENIChomozygous112736368