chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144193482144193483CT17GENIChomozygous112869499
4144193505144193506TA19GENIChomozygous112869500
4144193508144193509TG20GENIChomozygous112869501
4144193513144193514CA19GENIChomozygous112869502
4144193518144193519TA19GENIChomozygous112869503
4144202944144202944C21GENIChomozygous128087478
4144208989144208990AT14GENIChomozygous112869532
4144208998144208999AT13GENIChomozygous113058720
4144208999144209000CT13GENIChomozygous113058722
4144209007144209008CA12GENIChomozygous113058724
4144209008144209009TG12GENIChomozygous113058726
4144209010144209011TC12GENIChomozygous113058728
4144209014144209015GC11GENIChomozygous112869533
4144209044144209045CT13GENIChomozygous112869534
4144209050144209051GA10GENIChomozygous112869535
4144209083144209084CA12GENIChomozygous119315054
4144209087144209088GA13GENIChomozygous119315056
4144209093144209094CT15GENIChomozygous113562700
4144209097144209098GC15GENIChomozygous119315058
4144209101144209102CA17GENIChomozygous119315060
4144209102144209103TG17GENIChomozygous119315062
4144209120144209121AC17GENIChomozygous112869536
4144209121144209122GC18GENIChomozygous112869537
4144213140144213140T11GENIChomozygous128087488
4144209084144209085TG12GENIChomozygous119281598
4144209086144209087TC13GENIChomozygous119281600