chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58238732182387322GA17GENIChomozygous55504305
58238794882387949AC27GENIChomozygous55504308
58238796582387966CT28GENIChomozygous55504311
58238819482388195GA24GENIChomozygous55504314
58238828282388283CCT13GENICheterozygous55504317
58238897482388975AG18GENIChomozygous55504319
58238909782389098CT17GENIChomozygous55504322
58238946682389467GC26GENIChomozygous55504325
58239045082390451GA22GENIChomozygous55504328
58239085282390853AT22GENIChomozygous55504330
58239123282391233CT11GENIChomozygous55504333
58239235782392358CT19GENIChomozygous55504336
58239254182392542TA24GENIChomozygous55504339
58239260782392608CT17GENIChomozygous55504342
58239321082393211AG31GENIChomozygous55504344
58239376982393770GA25GENIChomozygous55504346
58239382582393826CA32GENIChomozygous55504349
58239444782394448GA16GENIChomozygous55504352
58239480982394810AT22GENIChomozygous55504355
58239554282395543CT25GENIChomozygous55504358
58239597582395976GA28GENIChomozygous55504361
58239674882396749AG31GENIChomozygous55504364
58239766382397664AG37GENIChomozygous55504367
58239794382397944AG28GENIChomozygous55504369
58239822482398225TTAAG36GENICheterozygous55504372
58239824782398251CTCT----17GENIChomozygous55504375
58239950982399510CT28GENIChomozygous55504378