chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134446991244469913AG11GENIChomozygous114546777
134446994944469950AG11GENIChomozygous114546778
134446996344469964AC14GENIChomozygous114546779
134446996444469965GC13GENIChomozygous114546780
134447041944470420CT14GENIChomozygous114546781
134447042944470430CT12GENIChomozygous114546782
134447043744470438TA13GENIChomozygous114546783
134447121344471214CG11GENIChomozygous114546784
134447123544471236TG6GENIChomozygous114546785
134447130744471308AG7GENIChomozygous114546786
134447145644471457TC9GENIChomozygous114546787
134447149244471493AT14GENIChomozygous114546788
134447149944471500TC14GENIChomozygous114546789
134447150844471509GA14GENIChomozygous114546790
134447169244471693AC14GENIChomozygous114546791
134447169344471694GT14GENIChomozygous114546792
134447172644471727CT8GENIChomozygous114546793
134447191944471920TC13GENIChomozygous114546794
134447324344473244CG5GENIChomozygous114546795
134447330644473307AG6GENIChomozygous114546796
134447344644473447TC9GENICpossibly homozygous114546797
134447378144473782GA6GENIChomozygous114546798
134447381644473817AT4GENIChomozygous114546799
134447479644474797CT13GENIChomozygous114546800