chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181527229515272296TG37GENICpossibly homozygous110281698
181527233515272336T34GENIChomozygous129517794
181527244915272450AG30GENIChomozygous110281700
181527262215272622CTTCTC14GENIChomozygous129517795
181527307215273073T28GENIChomozygous129517796
181527334015273341GT45GENIChomozygous110281702
181527374915273750CT46GENIChomozygous110281704
181527375815273759TC45GENIChomozygous110281706
181527376315273764AC48GENIChomozygous110281708
181527380715273808AG49GENIChomozygous110281710
181527418015274181GC58GENIChomozygous110281712
181527420315274204AT54GENIChomozygous110281714
181527445815274459GA38GENIChomozygous110281716
181527510115275101GTG41GENIChomozygous129517797
181527536015275361A38GENIChomozygous129517798
181527536915275370C36GENIChomozygous129517799
181527537015275371TG34GENIChomozygous110525369
181527540715275408A11GENICheterozygous129517800
181527542915275430GA10GENIChomozygous124445535
181527546615275467G11GENIChomozygous129517801
181527550215275502CA16GENIChomozygous129517802
181527552115275522A18GENIChomozygous129517803
181527553215275532CACACACACTACATAC20GENIChomozygous129517804
181527563815275638ATTT32GENIChomozygous129517805
181527615915276159A35GENIChomozygous129517806
181527648815276496CCGTGGTC34GENIChomozygous129517807
181527549315275494GA15GENIChomozygous119482615
181527702915277029G48GENIChomozygous129517808
181527750715277507A50GENICpossibly homozygous129517809
181527316015273161GA34GENIChomozygous110644275
181527982515279826AG44GENIChomozygous110281718
181527983415279835TC48GENIChomozygous110281720
181528194015281941CT28GENIChomozygous110281722