chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107839206178392062CT22GENICpossibly homozygous116644140
107839219378392194TC32GENIChomozygous116644142
107839259078392591CA24GENIChomozygous116806613
107839277178392772CT30GENIChomozygous116806615
107839285378392854CT32GENIChomozygous116644144
107839322078393221TG22GENIChomozygous116644146
107839366278393663AG27GENIChomozygous116644148
107839471278394713TC29GENICpossibly homozygous116806617
107839493978394940TC27GENIChomozygous116644150
107839528278395283GA20GENIChomozygous116644154
107839566178395662TG24GENIChomozygous116644170
107839741778397418AG23GENIChomozygous116644182
107839751378397514AT19GENIChomozygous116806619
107840207378402074AG25GENIChomozygous116806621
107842073978420740AT38GENIChomozygous116806623
107842184678421847GA14GENIChomozygous116806627
107842362278423623AG17GENIChomozygous116806629
107842364978423650TC22GENIChomozygous116806631
107842368578423686TC27GENIChomozygous116806633
107842376478423765CG19GENIChomozygous116806635
107842463878424639GA36GENIChomozygous116806645
107842383778423838CG29GENIChomozygous116806637
107842437878424379TC31GENIChomozygous116806639
107842445078424451AG38GENICpossibly homozygous116806641
107842454178424542CT28GENIChomozygous116806643
107842717378427174AT11GENICpossibly homozygous116806647
107842721178427212TC27GENIChomozygous116806649
107842738978427390GC23GENIChomozygous116806651
107842801078428011AG17GENIChomozygous116806653
107842801178428012GT17GENIChomozygous116806655
107842896678428967TC24GENIChomozygous116644302
107842900378429004AG24GENIChomozygous116644304
107843315678433157GT24GENIChomozygous116806665
107843455678434557AT25GENIChomozygous116806669
107843457178434572CT36GENIChomozygous116806671
107843486878434869TC23GENIChomozygous116806673
107843500178435002TC32GENIChomozygous116806675
107843506178435062AG17GENIChomozygous116806677