chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105957090159570902GC28GENIChomozygous51465802
105957098159570982GA28GENIChomozygous51465803
105957105259571053CA27GENIChomozygous51465804
105957120559571206CT25GENIChomozygous51465805
105957154559571546TC25GENIChomozygous51465806
105957190759571908GA44GENIChomozygous51465807
105957209059572091GT33GENIChomozygous51465808
105957215959572160TC36GENIChomozygous51465809
105957232059572321CT23GENIChomozygous51465810
105957363259573633GT32GENIChomozygous51465811
105957408459574085AT20GENIChomozygous51465812
105957422759574232AAACC-----21GENIChomozygous51465813
105957652659576527GA36GENIChomozygous51465815
105957714959577150AG38GENIChomozygous51465816
105957736059577361TA24GENIChomozygous52062462
105957736159577362TA24GENIChomozygous52062464
105957848959578490AATT17GENICheterozygous51465818
105957848959578490AATTT17GENICpossibly homozygous52503410
105957914259579143TC41GENIChomozygous51465819
105957962659579627AG30GENIChomozygous51465820
105957974259579743TG30GENIChomozygous51465821
105958012659580127CT26GENIChomozygous51465822
105958190359581904TC14GENIChomozygous51465823
105958215659582157AG27GENIChomozygous51465825
105958267159582672CCA41GENIChomozygous51465826
105958318959583190TC22GENIChomozygous51465827
105958442159584422AAGT9GENICheterozygous51465828
105958442159584422AAGTGT9GENICheterozygous52379144
105958446559584466TC21GENIChomozygous51465829
105958453359584535TG--27GENIChomozygous51465830
105958468159584682A-27GENIChomozygous51465831
105958490259584903TC23GENIChomozygous51465832
105958711059587111CT18GENIChomozygous51465833
105958767859587679CT29GENIChomozygous51465834
105958976759589768TC25GENIChomozygous51465835
105959129359591300GGCATTT-------17GENIChomozygous51465836
105959166359591664CCTCTCTCTCTGTGTGTGTGTGTG10GENICpossibly homozygous52460893
105959390759593908TC28GENIChomozygous51465837
105959710559597106GGC16GENICpossibly homozygous51465838
105959928459599285GT28GENIChomozygous51465839
105960012859600129G-33GENIChomozygous51465841