chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97967276079672760TGTTC19GENIChomozygous128726900
97967358779673597TCCCCGCTCA7GENIChomozygous128726901
97967361079673611T11GENIChomozygous128726902
97967361579673615A12GENIChomozygous128726903
97967362979673632GGG14GENIChomozygous128726904
97967363679673637G14GENIChomozygous128726905
97967366779673668AT23GENIChomozygous117809024
97967366979673670C23GENIChomozygous128726906
97967367679673678TA25GENIChomozygous128726907
97967368079673682CC26GENIChomozygous128726908
97967369179673691C32GENIChomozygous128726909
97967369679673696T34GENIChomozygous128726910
97967370879673708T36GENIChomozygous128726911
97967371679673716C41GENIChomozygous128726912
97972742879727429G23GENIChomozygous128726913
97972743179727432G23GENIChomozygous128726914
97972749779727498A10GENIChomozygous128726915
97972750279727503A10GENIChomozygous128726916
97972750879727509GA9GENIChomozygous117380750
97972751279727513TG9GENIChomozygous117380751
97972753879727539C7GENIChomozygous128726917
97972758579727585C10GENIChomozygous128726918
97972760279727603C9GENIChomozygous128726919
97972761679727617GT10GENIChomozygous123203952
97972761779727618TG10GENIChomozygous123203953
97972763279727633AT13GENIChomozygous123203954
97972763379727634TA13GENIChomozygous123203955
97972766579727665A11GENIChomozygous128726920
97972767579727676TA13GENIChomozygous123203960
97972769079727691GA15GENIChomozygous117594054
97972769179727692AG17GENIChomozygous123203962
97973668879736689C50GENIChomozygous128726923
97972766779727668G11GENIChomozygous128726921
97972767779727678C13GENIChomozygous128726922
97973283479732834T66GENICheterozygous130379738
97973669279736693C51GENIChomozygous128726924
97974656079746561CA24GENIChomozygous128774622