chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181527229515272296TG16GENIChomozygous110281698
181527233515272336T11GENIChomozygous129517794
181527244915272450AG13GENIChomozygous110281700
181527262215272622CTTCTC8GENIChomozygous129517795
181527307215273073T12GENIChomozygous129517796
181527334015273341GT17GENIChomozygous110281702
181527374915273750CT14GENIChomozygous110281704
181527375815273759TC14GENIChomozygous110281706
181527376315273764AC14GENIChomozygous110281708
181527380715273808AG15GENIChomozygous110281710
181527418015274181GC18GENIChomozygous110281712
181527420315274204AT19GENIChomozygous110281714
181527445815274459GA16GENIChomozygous110281716
181527510115275101GTG12GENIChomozygous129517797
181527316015273161GA12GENIChomozygous110644275
181527536015275361A18GENIChomozygous129517798
181527536915275370C17GENIChomozygous129517799
181527537015275371TG17GENIChomozygous110525369
181527540715275408A5GENIChomozygous129517800
181527542915275430GA6GENIChomozygous124445535
181527546615275467G11GENIChomozygous129517801
181527549315275494GA8GENIChomozygous119482615
181527550215275502CA9GENIChomozygous129517802
181527552115275522A11GENIChomozygous129517803
181527553215275532CACACACACTACATAC14GENIChomozygous129517804
181527563815275638ATTT15GENIChomozygous129517805
181527615915276159A6GENIChomozygous129517806
181527648815276496CCGTGGTC14GENIChomozygous129517807
181527702915277029G23GENIChomozygous129517808
181527750715277507A18GENIChomozygous129517809
181527982515279826AG12GENIChomozygous110281718
181527983415279835TC11GENIChomozygous110281720
181528194015281941CT14GENIChomozygous110281722