chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113075601830756019AAGGTTT14GENIChomozygous50715679
113075628930756290CCA28GENIChomozygous50715680
113075656330756564G-4GENICheterozygous50715681
113075712830757132TTTT----11GENIChomozygous50715685
113075796430757965CCT5GENICheterozygous50715687
113075796530757966T-5GENICheterozygous50715688
113076065630760657AG15GENIChomozygous50715689
113076080230760803AC16GENIChomozygous50715690
113076191230761913TTG31GENIChomozygous50715691
113076274130762742AG43GENIChomozygous50715692
113076307330763074GT29GENIChomozygous50715693
113076391230763913TTA9GENICpossibly homozygous50715694
113076517330765174AC24GENIChomozygous50715695
113076648030766481AAAAATAAATAAATAAAT1GENIChomozygous51275151
113076666330766664GA13GENIChomozygous50715696
113076681930766820CT31GENIChomozygous50715697