chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23495199334951994GA23GENIChomozygous125718037
23495392234953923GA20GENIChomozygous125718038
23495645934956460AG21GENIChomozygous110683244
23495661734956618TC13GENIChomozygous110683246
23495675334956754AT15GENIChomozygous125718039
23495704634957047AT8GENIChomozygous125718040
23495712634957127CA16GENIChomozygous125718041
23495738934957390CT11GENIChomozygous109690586
23495761134957612TC15GENIChomozygous109690588
23495778434957785CA28GENIChomozygous109690590
23495805834958059TC20GENIChomozygous109690592
23495835434958355TC12GENIChomozygous109690594
23495837934958380CT9GENIChomozygous109690596
23495839034958391AC9GENIChomozygous109690598
23495854634958547AG24GENIChomozygous109690600
23495860034958601CA24GENIChomozygous125718042
23495866834958669TC12GENIChomozygous109690602
23495868734958688TC14GENIChomozygous109690604
23495871234958713AG8GENIChomozygous109690606
23495873534958736TC16GENIChomozygous109690607
23495943334959434TC9GENIChomozygous109690609
23495943934959440AG9GENIChomozygous109690611
23495947434959475GA19GENIChomozygous109690613
23495972134959722GA26GENIChomozygous109690615
23496030334960304AG26GENIChomozygous125718043
23496038534960386GT21GENICheterozygous125718044
23496234734962348TC18GENIChomozygous109690619
23496397434963975GA19GENIChomozygous110683250
23496418134964182TC10GENIChomozygous109690625
23496439334964394CT20GENIChomozygous110683252
23496474934964750TC15GENIChomozygous109690627
23496489034964891AG10GENIChomozygous125718045
23496490634964907CA15GENIChomozygous109690629