chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213134682131347C-1GENIChomozygous51516669
108213362782133628A-7GENICpossibly homozygous52068528
108213769082137691C-4GENICheterozygous51516710
108213896182138962GT2GENIChomozygous52390726
108213897882138979GT1GENIChomozygous51516720
108213898382138984CT1GENIChomozygous51516721
108213899882138999GT1GENIChomozygous51516722
108213900082139001AT1GENIChomozygous51516723
108213900782139008AT1GENIChomozygous51516724
108213901982139020AT4GENIChomozygous51516725
108213917182139172A-7GENICheterozygous51516727
108213925882139259CG2GENIChomozygous51516729
108213926282139263AAG2GENICheterozygous51516730
108213926882139269A-4GENICheterozygous51516731
108215106182151063AC--6INTERGENICheterozygous52068545
108215503282155033T-1GENIChomozygous51516783
108216395382163957AACC----20INTERGENICheterozygous52444014
108216397582163976CT14INTERGENICheterozygous51516809
108218548182185482CCA20GENICpossibly homozygous51516834
108218853682188537C-6GENICheterozygous52570465