chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186898892968988930T44GENICpossibly homozygous140230450
186898917068989171GT35GENIChomozygous140345741
186899009068990091GT35GENIChomozygous140345742
186899191568991916GA39GENIChomozygous140345743
186899251068992520CTGCATTCAA40GENIChomozygous140230451
186899431168994312TG55GENIChomozygous140345744
186899826368998264AC57GENICpossibly homozygous140345745
186899838468998385AG48GENIChomozygous140345746
186900053669000536TCTAGAG30GENIChomozygous140230452
186900081269000813AG35GENIChomozygous140345747
186900096869000969TC50GENIChomozygous140345748
186900131969001320CG48GENIChomozygous140345749
186900137169001372AG58GENIChomozygous140345750
186900282069002821AG39GENIChomozygous140345751
186900353769003537G62GENIChomozygous140230453
186900379469003795TC47GENIChomozygous140345752
186900397769003977T44GENIChomozygous140230454
186900421569004215TTTTTG20GENICheterozygous140230455
186900461569004616CG54GENIChomozygous140345753
186900534969005350CT60GENIChomozygous140345754
186900637869006379AG50GENICpossibly homozygous140345755
186900691969006931GGGGGTTAGGGT45GENIChomozygous140230456
186900852069008521TC50GENIChomozygous140345756
186900857369008574GC50GENIChomozygous140345757
186900923669009237GA42GENIChomozygous140345758
186900955169009552TG36GENIChomozygous140345759
186900958069009581CT40GENIChomozygous140345760
186900963769009637GTGTGA45GENIChomozygous140230458
186901024469010245AC34GENIChomozygous140345761
186901032369010324GA40GENIChomozygous140345762
186901069269010693TC37GENIChomozygous140345763
186901165469011655AG45GENIChomozygous140345764
186901174069011741TC47GENIChomozygous140345765
186901191169011911ATT52GENIChomozygous140230459
186901296069012960TC50GENIChomozygous140230460
186901302369013024GA51GENIChomozygous140345766
186900574469005745GA56GENIChomozygous155060092
186900574469005745GC56GENICheterozygous403438931
186900731269007313A10GENICheterozygous140230457
186900731269007313AC10GENIChomozygous155060093