chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107839206178392062CT13GENIChomozygous116644140
107839219378392194TC30GENIChomozygous116644142
107839259078392591CA23GENIChomozygous116806613
107839277178392772CT24GENIChomozygous116806615
107839285378392854CT22GENIChomozygous116644144
107839322078393221TG27GENIChomozygous116644146
107839366278393663AG22GENIChomozygous116644148
107839404878394049GA12GENIChomozygous117104813
107839471278394713TC20GENIChomozygous116806617
107839493978394940TC23GENIChomozygous116644150
107839528278395283GA34GENIChomozygous116644154
107839566178395662TG26GENIChomozygous116644170
107839741778397418AG23GENIChomozygous116644182
107842073978420740AT27GENIChomozygous116806623
107840207378402074AG11GENIChomozygous116806621
107842184678421847GA23GENIChomozygous116806627
107842362278423623AG22GENIChomozygous116806629
107842364978423650TC21GENIChomozygous116806631
107842368578423686TC20GENIChomozygous116806633
107842376478423765CG17GENIChomozygous116806635
107842383778423838CG21GENIChomozygous116806637
107842437878424379TC24GENIChomozygous116806639
107842445078424451AG28GENIChomozygous116806641
107842454178424542CT24GENIChomozygous116806643
107842463878424639GA24GENIChomozygous116806645
107842738978427390GC19GENIChomozygous116806651
107842801078428011AG24GENIChomozygous116806653
107842801178428012GT25GENIChomozygous116806655
107842896678428967TC28GENIChomozygous116644302
107842900378429004AG31GENIChomozygous116644304
107842974878429749CT30GENIChomozygous116806657
107842975078429751CT30GENIChomozygous116806659
107843269278432693AC32GENIChomozygous116806661
107843301678433017GA23GENIChomozygous116806663
107843315678433157GT21GENIChomozygous116806665
107843455678434557AT24GENIChomozygous116806669
107843457178434572CT26GENIChomozygous116806671
107843486878434869TC27GENIChomozygous116806673
107843500178435002TC25GENIChomozygous116806675