chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150204129150204130CG21GENIChomozygous56980459
4150204938150204939AG24GENIChomozygous56980460
4150205872150205873CA24GENIChomozygous56980461
4150206402150206403CT22GENIChomozygous56980462
4150206578150206579TC29GENIChomozygous56980463
4150207020150207021AG20GENIChomozygous56980464
4150207128150207162GTATATATATATATATATATATATATATATATAT----------------------------------17GENICheterozygous58473650
4150207128150207160GTATATATATATATATATATATATATATATAT--------------------------------17GENICheterozygous58660712
4150208551150208552GA13GENIChomozygous56980465
4150208762150208763TC6GENIChomozygous56980466
4150209380150209381GA28GENIChomozygous56980467
4150209497150209499AA--8GENICheterozygous58473652
4150209498150209499A-8GENICpossibly homozygous58473654
4150210105150210106TA36GENIChomozygous56980469
4150210239150210240CT30GENIChomozygous56980470
4150210852150210853TC19GENIChomozygous56980471
4150210990150210991TC26GENIChomozygous56980472
4150211010150211011TA26GENIChomozygous56980473
4150211732150211733AAC21GENICpossibly homozygous56980474
4150212444150212445CA32GENIChomozygous56980475
4150212629150212630GA43GENIChomozygous56980476
4150212756150212757GA46GENIChomozygous56980477
4150213841150213842GA27GENIChomozygous56980478
4150214114150214115CT21GENIChomozygous56980479
4150214698150214699TC28GENIChomozygous56980480
4150215385150215386CT19GENIChomozygous56980481
4150215389150215390GA19GENIChomozygous56980482