chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162110102021101022AA--6GENICheterozygous47329573
162110509821105099CCT2GENICheterozygous47986770
162110642421106428TTTG----8GENIChomozygous47329614
162110661621106617TTC11GENIChomozygous47329616
162110746821107469CCTTGTCATGTA15GENIChomozygous47329622
162110757821107579CCA6GENIChomozygous47741317
162110837721108379TT--3GENIChomozygous47741319
162111207421112075AAT6GENICheterozygous47329651
162111292121112922TA28GENIChomozygous47329653
162111368721113688CCTTTTTTTTTTTTT15GENICheterozygous47924437
162111368821113689T-15GENICheterozygous47924438
162111462421114625TC8GENIChomozygous47741325
162111497221114977TCCTT-----1GENIChomozygous47924439
162111498021115001CGTATACTCCACCCCTGTTAC---------------------1GENIChomozygous47924440
162111572521115726GGCC3GENIChomozygous47741327
162111624221116254GACGGCATTAAC------------28GENICheterozygous47924441
162111788421117886TC--5GENICheterozygous47924443
162111825921118260CG10GENIChomozygous47741329
162112335221123353CT12GENICpossibly homozygous47741331
162112349721123498AG17GENIChomozygous47329709
162112702021127021T-14GENIChomozygous47741333
162112776221127776TTTTTTTTTTTTTT--------------4GENIChomozygous47986771
162112779821127799GT5GENIChomozygous47329736