chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150204129150204130CG20GENIChomozygous56980459
4150204938150204939AG21GENIChomozygous56980460
4150205872150205873CA19GENIChomozygous56980461
4150206402150206403CT21GENIChomozygous56980462
4150206578150206579TC22GENIChomozygous56980463
4150207020150207021AG18GENIChomozygous56980464
4150208551150208552GA20GENIChomozygous56980465
4150208762150208763TC12GENIChomozygous56980466
4150209380150209381GA21GENIChomozygous56980467
4150209497150209498A-2GENIChomozygous56980468
4150209510150209514AAAG----11GENICheterozygous57518644
4150210105150210106TA24GENIChomozygous56980469
4150210239150210240CT27GENIChomozygous56980470
4150210852150210853TC16GENIChomozygous56980471
4150210990150210991TC28GENIChomozygous56980472
4150211010150211011TA24GENIChomozygous56980473
4150211732150211733AAC8GENICheterozygous56980474
4150212444150212445CA15GENIChomozygous56980475
4150212629150212630GA14GENIChomozygous56980476
4150212756150212757GA14GENICpossibly homozygous56980477
4150213841150213842GA21GENIChomozygous56980478
4150214114150214115CT24GENIChomozygous56980479
4150214698150214699TC15GENIChomozygous56980480
4150215385150215386CT25GENIChomozygous56980481
4150215389150215390GA24GENIChomozygous56980482