chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57900607179006072AT49GENIChomozygous143238665
57900698779007008TTTGACCTCTCAATGCACAAG60GENIChomozygous137319110
57900703579007036AG70GENIChomozygous137519325
57900770579007706AT81GENIChomozygous137519326
57900855179008552GT53GENIChomozygous143238666
57900864579008646TC62GENIChomozygous137519327
57900891579008916GA58GENIChomozygous143238667
57901175379011754CT60GENIChomozygous143238668
57901186779011868AG54GENIChomozygous137519329
57901408379014084AG64GENIChomozygous137519330
57901558379015584AC56GENICpossibly homozygous137519333
57901572779015728GA64GENIChomozygous137519334
57901576679015767GA63GENIChomozygous143238669
57901580579015806TC53GENIChomozygous143238670
57901151379011514C42GENIChomozygous143182744
57901612479016130TTCTGC53GENIChomozygous143182745