chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186898892968988930T15GENIChomozygous140230450
186898917068989171GT18GENIChomozygous140345741
186899009068990091GT15GENIChomozygous140345742
186899191568991916GA18GENIChomozygous140345743
186899251068992520CTGCATTCAA10GENIChomozygous140230451
186899431168994312TG17GENIChomozygous140345744
186899826368998264AC19GENIChomozygous140345745
186899838468998385AG20GENIChomozygous140345746
186900053669000536TCTAGAG18GENIChomozygous140230452
186900081269000813AG23GENIChomozygous140345747
186900096869000969TC15GENIChomozygous140345748
186900131969001320CG20GENIChomozygous140345749
186900137169001372AG18GENIChomozygous140345750
186900282069002821AG24GENIChomozygous140345751
186900353769003537G25GENIChomozygous140230453
186900379469003795TC16GENIChomozygous140345752
186900397769003977T14GENIChomozygous140230454
186900421569004215TTTTTG14GENIChomozygous140230455
186900461569004616CG11GENIChomozygous140345753
186900534969005350CT14GENIChomozygous140345754
186900637869006379AG19GENIChomozygous140345755
186900852069008521TC15GENIChomozygous140345756
186900857369008574GC20GENIChomozygous140345757
186900923669009237GA15GENIChomozygous140345758
186900955169009552TG6GENIChomozygous140345759
186900958069009581CT8GENIChomozygous140345760
186901024469010245AC16GENIChomozygous140345761
186901032369010324GA15GENIChomozygous140345762
186901069269010693TC9GENIChomozygous140345763
186901165469011655AG18GENIChomozygous140345764
186901174069011741TC20GENIChomozygous140345765
186901296069012960TC10GENIChomozygous140230460
186900574469005745GA19GENIChomozygous155060092
186900574469005745GC19GENICheterozygous403438931
186900691969006931GGGGGTTAGGGT17GENIChomozygous140230456
186900731269007313A4GENIChomozygous140230457
186900963769009637GTGTGA18GENIChomozygous140230458
186901191169011911ATT16GENIChomozygous140230459
186901302369013024GA11GENIChomozygous140345766