chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150959674150959675AG30GENIChomozygous143968479
5150959744150959745GT28GENIChomozygous137651472
5150959803150959804AG24GENIChomozygous143968480
5150960064150960065T20GENIChomozygous141139266
5150960147150960148GT16GENIChomozygous143968481
5150960556150960598AAACGAACCTTCTTGGTTGTCTGCTGCGAGCCCCAGGCCTTA14GENIChomozygous148167404
5150960899150960900AC22GENIChomozygous143968482
5150961029150961030GA22GENIChomozygous143968483
5150961091150961092AG26GENIChomozygous143968484
5150961172150961173TC23GENIChomozygous143968485
5150961251150961251T19GENIChomozygous148167405
5150961602150961603T30GENIChomozygous148167406
5150961761150961762AG18GENIChomozygous143968486
5150961840150961841TC13GENIChomozygous137651474
5150962358150962359AG24GENIChomozygous143968487
5150962391150962392TC23GENIChomozygous143968488
5150962648150962649TC19GENIChomozygous143968490
5150962662150962663AG16GENIChomozygous137651477
5150962781150962782AG17GENIChomozygous143968491
5150962806150962807CT18GENIChomozygous143968492
5150963181150963182CT13GENIChomozygous143968493
5150963348150963349GA17GENIChomozygous137651478
5150966211150966211CACTTGGAATC15GENIChomozygous148167407
5150967818150967819CT10GENIChomozygous143968497
5150967837150967837ATAC11GENIChomozygous148167408
5150968430150968431AG25GENIChomozygous148169636
5150968477150968478AG27GENIChomozygous148169637
5150968586150968587TA17GENIChomozygous148169638
5150969291150969292GA15GENIChomozygous137651485
5150971310150971311AG26GENIChomozygous137651487
5150973046150973047GA21GENIChomozygous148169639
5150975457150975458GA14GENIChomozygous137651489
5150976880150976881TA15GENIChomozygous137651490
5150980944150980945GA15GENIChomozygous137651492
5150981177150981178AG8GENIChomozygous137651494