chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78311432183114322AG17GENIChomozygous116204693
78311434283114343TC21GENIChomozygous116204695
78311478283114783CG10GENIChomozygous116204697
78311504583115046AT18GENIChomozygous116204699
78311557283115573CT18GENIChomozygous116204701
78311558883115589GA16GENIChomozygous116204703
78311571783115718CT14GENIChomozygous116204705
78311590083115901CT18GENIChomozygous116204707
78311613883116139CA16GENIChomozygous116204709
78311635683116357TA25GENIChomozygous116204711
78311643283116433TG16GENIChomozygous116204713
78311702183117022TC17GENIChomozygous116204715
78311760883117609CT10GENIChomozygous116204717
78311811883118119CA18GENIChomozygous116204719
78311815883118159AC13GENIChomozygous116204721
78311822583118226TG17GENIChomozygous116204723
78311832983118330AC19GENIChomozygous116204725
78311837483118375GA20GENIChomozygous116204727
78311875983118760GA18GENIChomozygous116204729
78311954683119547CA15GENIChomozygous116204731
78311964783119648CT12GENIChomozygous116204733
78311965383119654AG12GENIChomozygous116204735
78312053283120533GC11GENIChomozygous116204737
78311551783115518T17GENIChomozygous132656006
78311735883117359A22GENIChomozygous132656007
78312222083122220TCCCCTAACCTAAACCCAAGCT14GENIChomozygous132656008
78311610083116101GA12GENIChomozygous115728361
78312214183122141ACAAACC19GENIChomozygous128486926
78312319483123195TC15GENIChomozygous116204743
78312413383124149TTCATCCGAAGGCATC12GENIChomozygous132656009
78312505983125060CT12GENIChomozygous116204745
78312543883125439AG22GENIChomozygous115728366
78312543983125440AC22GENIChomozygous115728367
78312544483125445AC22GENIChomozygous115728368
78312624183126242CT12GENIChomozygous116204747
78312708983127090TC13GENIChomozygous115728369
78312887583128876CT19GENIChomozygous116204750
78314789283147906TGAATCCTTCCAGC14GENIChomozygous132656010
78312544083125441AC22GENIChomozygous116046769