chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99416494794164948AG16GENIChomozygous117604745
99416509394165094CT13GENIChomozygous117601827
99416582894165835GACGAGC10GENIChomozygous132135222
99416648194166482CT19GENIChomozygous117604747
99416678294166783GA16GENIChomozygous117604749
99416802894168029CT18GENIChomozygous117601831
99416850194168502AG18GENIChomozygous117604753
99416911094169111GA18GENIChomozygous117601833
99416953094169531GT19GENIChomozygous117601835
99417017394170174AG21GENICpossibly homozygous117601837
99417163494171635AT15GENIChomozygous117601839
99417216694172167TC15GENIChomozygous117604759
99417218594172186TC16GENIChomozygous117604761
99417284094172841AG14GENIChomozygous117601841
99417574694175747AG13GENIChomozygous117601845
99417610894176109AG17GENIChomozygous117604769
99417671594176716TA16GENIChomozygous117601847
99417823794178240TGC25GENIChomozygous132135223
99417999894179999CT13GENIChomozygous117601849
99418000594180006TA12GENIChomozygous117601851
99418010994180110AG7GENIChomozygous117390000
99418011394180114CA7GENIChomozygous117390002
99418090894180909GA9GENIChomozygous117601853
99418111694181117CT18GENIChomozygous117601855
99418144394181444AG14GENIChomozygous117390003
99418161594181615TACA10GENIChomozygous131894203
99416933594169335A14GENIChomozygous128733174
99417920294179206AAAC23GENIChomozygous128733176
99418302294183023TC18GENIChomozygous117604775
99418323794183238GA12GENIChomozygous117604777
99418397594183975C7GENIChomozygous132135224
99418404594184046GA12GENIChomozygous117601859
99418476494184765AG12GENIChomozygous117604781
99418490094184901GA16GENIChomozygous117604783