chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-9GENIChomozygous51516668
108213134682131347C-9GENIChomozygous51516669
108213449582134496GT14GENICpossibly homozygous51516690
108213769082137691C-5GENIChomozygous51516710
108213897882138979GT18GENIChomozygous51516720
108213898382138984CT19GENIChomozygous51516721
108213899882138999GT20GENIChomozygous51516722
108213900082139001AT20GENIChomozygous51516723
108213900782139008AT22GENIChomozygous51516724
108213901982139020AT22GENIChomozygous51516725
108213919582139196A-9GENICheterozygous51516728
108213925882139259CG13GENIChomozygous51516729
108213926282139263AAG13GENIChomozygous51516730
108213926882139269A-13GENIChomozygous51516731
108214391782143918T-14GENICheterozygous51516747
108213896182138962GT13GENIChomozygous52390726
108214765382147654T-14INTERGENICheterozygous52461990
108215116782151168A-7INTERGENICheterozygous52506282
108216039082160391TG20INTERGENIChomozygous51516792
108216039182160392TA20INTERGENIChomozygous51516793
108216039682160397C-20INTERGENIChomozygous51516794
108216039782160398CG20INTERGENIChomozygous52390728
108216161582161616G-21INTERGENICheterozygous51516802
108217032182170325TATG----17INTERGENIChomozygous51717210
108217776782177768CCT4GENICheterozygous52390732
108218548182185482CCA11GENIChomozygous51516834