chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1786130108613011TC23GENIChomozygous110949668
1786136408613641GA35GENIChomozygous110949669
1786156978615698AG23GENIChomozygous111165948
1786157138615714GA13GENIChomozygous111229157
1786157448615745GA16GENIChomozygous111229159
1786157818615782GA21GENIChomozygous110949673
1786157948615795TC26GENIChomozygous110949674
1786159758615976AC27GENIChomozygous110949677
1786163058616306CT29GENIChomozygous110949678
1786167718616772AG17GENIChomozygous110949679
1786171328617133AG23GENIChomozygous110949680
1786179688617969AT25GENIChomozygous110949681
1786180528618053GC28GENIChomozygous110949682
1786180808618081TC24GENIChomozygous110949683
1786184208618421AG36GENIChomozygous110949684
1786184988618499AG20GENIChomozygous110949685
1786185008618501GA20GENIChomozygous110949686
1786186988618699CT26GENIChomozygous110949687
1786188998618900GA33GENIChomozygous110949688
1786194468619447TC34GENIChomozygous110949689
1786194478619448GA34GENIChomozygous110949690
1786200118620012AG22GENIChomozygous110949691
1786202808620281CT29GENIChomozygous110949692
1786205418620542TC34GENIChomozygous110949693
1786208658620866GA28GENIChomozygous110949694
1786209128620913TC37GENIChomozygous110949695
1786217818621782TC18GENIChomozygous111294834
1786219718621972CG28GENIChomozygous110949697
1786220148622015TC28GENIChomozygous110949698
1786234738623474GA42GENIChomozygous110949700
1786237338623734AG23GENIChomozygous110949701
1786240078624008TG18GENIChomozygous110949705
1786240558624056CT30GENIChomozygous110949707
1786249028624903GA28GENIChomozygous110949708