chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101415231414152315T24GENICheterozygous141036921
101415269814152699TG30GENIChomozygous142218534
101415378114153782GA32GENIChomozygous142218535
101415467814154679AG28GENIChomozygous142218536
101415472014154721CT34GENIChomozygous142218537
101415641614156417GA20GENIChomozygous142218538
101415741814157419AC23GENIChomozygous142218539
101415768014157681AG29GENIChomozygous142218540
101415768314157684AG30GENIChomozygous142218541
101415857214158686GGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTGTAGCCC24GENIChomozygous142196926
101415980614159807TC24GENIChomozygous142218542
101415994014159941G23GENIChomozygous142196927
101416066814160669AG28GENIChomozygous142218543
101416090114160902TC20GENIChomozygous142218544
101416090414160904GCACCAACACT19GENIChomozygous142196928
101416125514161256AG11GENIChomozygous142218545
101416235314162354GC22GENIChomozygous142218546
101416377714163778CA25GENIChomozygous142218547
101416469314164694TG27GENIChomozygous142218548
101416807514168076AG28GENIChomozygous142218549
101416926814169269TA22GENIChomozygous142218550
101417164914171650A15GENICheterozygous403276928
101415769814157699TA28GENICheterozygous154679902
101415769814157699T28GENICpossibly homozygous403276927
101417164914171650AT15GENICheterozygous154679907
101417485614174857GT29GENIChomozygous142218551
101417500414175005TA27GENIChomozygous142218552
101417645714176458AG22GENIChomozygous142218553