chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58238732182387322GA33GENIChomozygous55504305
58238794882387949AC20GENIChomozygous55504308
58238796582387966CT18GENIChomozygous55504311
58238819482388195GA22GENIChomozygous55504314
58238828282388283CCT18GENICpossibly homozygous55504317
58238897482388975AG13GENIChomozygous55504319
58238909782389098CT22GENIChomozygous55504322
58238946682389467GC27GENIChomozygous55504325
58239045082390451GA23GENIChomozygous55504328
58239085282390853AT28GENIChomozygous55504330
58239123282391233CT20GENIChomozygous55504333
58239235782392358CT38GENIChomozygous55504336
58239254182392542TA32GENIChomozygous55504339
58239260782392608CT29GENIChomozygous55504342
58239321082393211AG28GENIChomozygous55504344
58239376982393770GA28GENIChomozygous55504346
58239382582393826CA34GENIChomozygous55504349
58239444782394448GA29GENIChomozygous55504352
58239480982394810AT30GENIChomozygous55504355
58239554282395543CT30GENIChomozygous55504358
58239597582395976GA20GENIChomozygous55504361
58239674882396749AG28GENICpossibly homozygous55504364
58239766382397664AG31GENIChomozygous55504367
58239794382397944AG22GENIChomozygous55504369
58239822482398225TTAAGACC4GENIChomozygous56429725
58239822582398226TTACCTA4GENIChomozygous56429727
58239824782398248CCT4GENIChomozygous56429729
58239825082398251TTTTCCTTCCTTC4GENIChomozygous56429731
58239950982399510CT37GENIChomozygous55504378