chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101415269814152699TG56GENIChomozygous142218534
101415378114153782GA67GENIChomozygous142218535
101415467814154679AG44GENIChomozygous142218536
101415472014154721CT56GENIChomozygous142218537
101415641614156417GA44GENIChomozygous142218538
101415741814157419AC65GENIChomozygous142218539
101415768014157681AG49GENIChomozygous142218540
101415768314157684AG47GENIChomozygous142218541
101415769814157699TA46GENICheterozygous154679902
101415769814157699T46GENIChomozygous403276927
101415857214158686GGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTGTAGCCC36GENIChomozygous142196926
101415980614159807TC54GENIChomozygous142218542
101415994014159941G56GENIChomozygous142196927
101416066814160669AG54GENIChomozygous142218543
101416090114160902TC40GENIChomozygous142218544
101416090414160904GCACCAACACT41GENIChomozygous142196928
101416125514161256AG15GENIChomozygous142218545
101416235314162354GC49GENICpossibly homozygous142218546
101416377714163778CA58GENIChomozygous142218547
101416469314164694TG40GENIChomozygous142218548
101416807514168076AG67GENIChomozygous142218549
101416926814169269TA59GENIChomozygous142218550
101417485614174857GT53GENIChomozygous142218551
101417500414175005TA55GENIChomozygous142218552
101417645714176458AG63GENIChomozygous142218553
101417343314173434CT33GENIChomozygous146226692
101417164914171650AT25GENICheterozygous154679907
101417164914171650A25GENICpossibly homozygous403276928