chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204836556204836557AG13GENIChomozygous61063451
1204836728204836729GA13GENIChomozygous61063452
1204836737204836738AACTG8GENIChomozygous61063453
1204836739204836740AACT8GENIChomozygous61063454
1204836857204836858GGCAGCC18GENIChomozygous61063455
1204837027204837028AG16GENIChomozygous61063456
1204837242204837243GA12GENIChomozygous61063457
1204837636204837637AG8GENIChomozygous61063458
1204838122204838123TC17GENIChomozygous61063459
1204838358204838359GT10GENIChomozygous61063460
1204838669204838670GC16GENIChomozygous61063461
1204838856204838857CT14GENIChomozygous61063462
1204842541204842542GA25GENIChomozygous61063464
1204842608204842609AAAG18GENIChomozygous61063465
1204842790204842791AT10GENIChomozygous62095796
1204843365204843366GA17GENIChomozygous61063468
1204843983204843984CG13GENIChomozygous61063469
1204844200204844201AG14GENIChomozygous61063470
1204844208204844209AC14GENIChomozygous61063471
1204844283204844284GT12GENIChomozygous62804008
1204844284204844285TC11GENIChomozygous62804009
1204844295204844296AC10GENIChomozygous61063472
1204844300204844301GT10GENIChomozygous61063473
1204844305204844306GT10GENIChomozygous61063474
1204844318204844319GC7GENIChomozygous61063475
1204844322204844323GT7GENIChomozygous61063476
1204844325204844326AT6GENIChomozygous61063477
1204844332204844333GA6GENIChomozygous61063478
1204844334204844335GT5GENIChomozygous61063479
1204844676204844677T-14GENIChomozygous61063487
1204844924204844925GT15GENIChomozygous61063488
1204845485204845486AG15GENIChomozygous61063489
1204847110204847111GA9GENIChomozygous61063490
1204847392204847393GA14GENIChomozygous61063491
1204849531204849532TC10GENIChomozygous61063493
1204850607204850608AC7GENIChomozygous61063496
1204851455204851456CG17GENIChomozygous61063504
1204851491204851492TC16GENIChomozygous61063505
1204852919204852920GA10GENIChomozygous61063506
1204853056204853057CT15GENIChomozygous61063507
1204853279204853280GA10GENIChomozygous61063508
1204854131204854132GGC18GENIChomozygous61063509