chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76537934265379343GT13GENIChomozygous628334815
76539039165390392T-5GENICheterozygous744482485
76540766565407666CG28GENIChomozygous628334816
76540774465407745CT28GENIChomozygous628334817
76540777765407778TTG32GENIChomozygous744482487
76541289765412899GT--13GENICheterozygous744482488
76541657265416573TTGACAAG19GENIChomozygous744482491
76542307765423078TTTTAG31GENIChomozygous744482492
76542349965423500CCA13GENICheterozygous744482495
76542350265423503A-13GENICheterozygous744482494
76544066565440666AAGT11GENICheterozygous744482497
76544066665440668GT--11GENICheterozygous744482496
76544079965440801AA--16GENICheterozygous744482499
76545827265458273CCAG14GENIChomozygous744482501
76546415865464160CA--1GENIChomozygous744482502
76547259665472597TTCA1GENIChomozygous744482505
76547434165474342TC12GENIChomozygous628334818
76547434365474344TC13GENIChomozygous628334819
76547434865474349GT13GENIChomozygous628334820
76547435165474352TC13GENIChomozygous628334821
76547436165474362GC14GENIChomozygous628334822
76547436365474364GC15GENIChomozygous628334823
76547442265474423TG11GENIChomozygous628334824
76547443765474438AT13GENIChomozygous628334825
76547444165474442TC13GENIChomozygous628334826
76547445365474454TG16GENIChomozygous628334827
76547445765474458AC15GENIChomozygous628334828
76547445965474460TC15GENIChomozygous628334829
76547446165474462GC17GENIChomozygous628334830
76547483865474839T-38GENIChomozygous744482506
76547627365476274G-6GENICheterozygous744482507
76547814365478145CA--6GENICheterozygous744482511
76547825065478251G-18GENIChomozygous744482512
76547849965478500TG1GENIChomozygous628334831
76548091765480919GT--4GENICheterozygous744482514
76548206865482069A-22GENIChomozygous744482515
76548298865482990AA--7GENICheterozygous744482516
76548298965482990A-7GENICheterozygous744482517
76548472665484727A-9GENICheterozygous744482519