chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150204129150204130CG49GENIChomozygous56980459
4150204938150204939AG56GENIChomozygous56980460
4150205872150205873CA41GENIChomozygous56980461
4150206402150206403CT49GENIChomozygous56980462
4150206578150206579TC42GENIChomozygous56980463
4150207020150207021AG43GENIChomozygous56980464
4150208551150208552GA65GENIChomozygous56980465
4150208762150208763TC20GENIChomozygous56980466
4150209380150209381GA26GENIChomozygous56980467
4150209497150209498A-5GENIChomozygous56980468
4150210105150210106TA44GENICpossibly homozygous56980469
4150210239150210240CT53GENIChomozygous56980470
4150210852150210853TC40GENIChomozygous56980471
4150210990150210991TC50GENIChomozygous56980472
4150211010150211011TA48GENIChomozygous56980473
4150211732150211733AAC7GENICheterozygous56980474
4150212444150212445CA45GENIChomozygous56980475
4150212629150212630GA39GENICpossibly homozygous56980476
4150212756150212757GA43GENICpossibly homozygous56980477
4150213841150213842GA40GENIChomozygous56980478
4150214114150214115CT48GENIChomozygous56980479
4150214698150214699TC46GENIChomozygous56980480
4150215385150215386CT41GENIChomozygous56980481
4150215389150215390GA38GENIChomozygous56980482