chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
66997593669975937AG21GENIChomozygous114848685
66997734369977344AC17GENIChomozygous114848686
66997751169977512GA30GENIChomozygous115406569
66997900169979002AT18GENIChomozygous115406571
66998009669980097GC23GENIChomozygous114848688
66998011469980115TA23GENIChomozygous114848689
66998127169981272TC29GENIChomozygous114848690
66998131569981316AT30GENIChomozygous115406572
66998159969981600GA19GENIChomozygous114848691
66998228469982285CT8GENIChomozygous114848697
66998465669984657GA24GENIChomozygous114848700
66998508369985084GA27GENIChomozygous114848701
66998563169985632GT13GENIChomozygous115406573
66998587669985877CT12GENIChomozygous114848702
66998746769987468AG21GENIChomozygous114848703
66998752069987521GA22GENIChomozygous114848704
66998761469987615TC18GENIChomozygous114848705
66998801569988016TC15GENIChomozygous114848706
66998853569988536TC10GENIChomozygous115406574
66998872569988726TC6GENIChomozygous115119948
66999071469990715TG8GENIChomozygous114848710
66998973569989736AC20GENIChomozygous114848708
66999046469990465CT31GENIChomozygous115406575
66999051469990515GA29GENIChomozygous115406576
66999082169990822CA21GENICpossibly homozygous114848711
66999088269990883TC18GENIChomozygous114848712
66999090369990904TC18GENIChomozygous115119954
66999095369990954GT19GENIChomozygous114848713
66999096069990961CT20GENIChomozygous115406577
66999155269991553TC16GENIChomozygous114848714
66999167869991679AT20GENIChomozygous115119956
66999169769991698CT27GENIChomozygous114848715
66999205869992059TC24GENIChomozygous114848716
66999220469992205CT15GENIChomozygous114848717
66999279169992792TC22GENIChomozygous114848720
66999315069993151CT30GENIChomozygous115406580
66999336169993362AG35GENIChomozygous114848721
66999353469993535GA31GENIChomozygous114848722
66999393269993933CG25GENIChomozygous114848723
66999405969994060GT27GENIChomozygous114848724
66999408269994083TG26GENIChomozygous114848725