chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135053227750532278CT8GENIChomozygous126066541
135053227950532280TC8GENIChomozygous126066542
135053375150533752AG6GENIChomozygous126066543
135053481750534818GA17GENIChomozygous126066544
135053661550536616TG9GENICheterozygous126066545
135053724550537246GA18GENIChomozygous126066546
135053778150537782AG8GENIChomozygous126066547
135053784750537848CT17GENIChomozygous126066548
135053885650538857TC15GENIChomozygous126066549
135053899650538997CT29GENIChomozygous126066550
135054226950542270CT13GENIChomozygous126066551
135054562550545626AC15GENIChomozygous126066552
135054610450546105CA12GENIChomozygous126066553
135054648650546487CT27GENIChomozygous126066554
135054832450548325AG14GENIChomozygous126066555
135054917350549174GA21GENIChomozygous126066556
135054949350549494AG17GENIChomozygous126066557
135055000750550008TC5GENIChomozygous126137929