chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14679240546792405T10GENIChomozygous127379759
14679248646792486CT14GENIChomozygous127379760
14679248846792491TCG14GENIChomozygous127379761
14679250746792507C15GENIChomozygous127379762
14679256246792562G17GENIChomozygous127379763
14679266046792660G15GENIChomozygous127379764
14679266246792662T16GENIChomozygous127379765
14679275246792752C19GENIChomozygous127379766
14679279446792794CTT20GENIChomozygous127379767
14679292246792922C29GENIChomozygous127379768
14679305146793052TC16GENIChomozygous109076234
14679308346793084G16GENIChomozygous127379769
14679311546793116G15GENIChomozygous127379770
14679313246793133G18GENIChomozygous127379771
14679321446793215A22GENIChomozygous127379772
14679323646793237C19GENIChomozygous127379773
14679329746793298T18GENIChomozygous127379774
14679338346793384A10GENIChomozygous127379775
14679290346792904AG28GENIChomozygous120471450
14679290446792905GA27GENIChomozygous120471451
14679304946793050CT16GENIChomozygous108721436
14679336346793364TC12GENIChomozygous108094145
14679722746797228TC6GENIChomozygous130523538
14680008246800083GA9GENICheterozygous130523539
14679982446799825GA8GENICheterozygous127533053
14680003346800034GA9GENICheterozygous130224845
14680258646802587T2GENIChomozygous127379776
14680270346802709ATATAA2GENIChomozygous127379777
14680276446802765GC4GENIChomozygous108721437
14682236946822369T17GENIChomozygous127379778