chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99416494794164948AG14GENIChomozygous117604745
99416509394165094CT24GENIChomozygous117601827
99416582894165835GACGAGC17GENIChomozygous132135222
99416648194166482CT18GENIChomozygous117604747
99416678294166783GA12GENIChomozygous117604749
99416802894168029CT16GENIChomozygous117601831
99416850194168502AG26GENIChomozygous117604753
99416911094169111GA23GENIChomozygous117601833
99416953094169531GT18GENIChomozygous117601835
99417017394170174AG22GENIChomozygous117601837
99417163494171635AT16GENIChomozygous117601839
99417216694172167TC15GENIChomozygous117604759
99417218594172186TC14GENIChomozygous117604761
99417284094172841AG15GENIChomozygous117601841
99417574694175747AG17GENIChomozygous117601845
99417610894176109AG22GENIChomozygous117604769
99417671594176716TA13GENIChomozygous117601847
99417823794178240TGC28GENIChomozygous132135223
99417999894179999CT15GENIChomozygous117601849
99418000594180006TA15GENIChomozygous117601851
99418090894180909GA17GENIChomozygous117601853
99418111694181117CT14GENIChomozygous117601855
99418144394181444AG16GENIChomozygous117390003
99418302294183023TC16GENIChomozygous117604775
99418323794183238GA14GENIChomozygous117604777
99418404594184046GA17GENIChomozygous117601859
99418476494184765AG24GENIChomozygous117604781
99418490094184901GA12GENICpossibly homozygous117604783
99416933594169335A17GENIChomozygous128733174
99418161594181615TACA15GENIChomozygous131894203
99418397594183975C15GENIChomozygous132135224
99417920294179206AAAC24GENIChomozygous128733176