chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101288104412881045AC6GENIChomozygous519362220
101288105112881052GC9GENICheterozygous519362221
101288108412881085AG14GENIChomozygous519362222
101288263112882635ATAT----3GENIChomozygous689464613
101288317012883171CCA9GENIChomozygous689464614
101288342812883432AAAC----2GENIChomozygous689464615
101288555912885560GT18GENIChomozygous516576858
101288586912885870TC14GENIChomozygous516576859
101288620912886210TG26GENICpossibly homozygous516576860
101288646712886468TC28GENICpossibly homozygous519362223
101288653112886532GA24GENICpossibly homozygous516576861
101288682512886826AG45GENIChomozygous516576862
101288705512887056GA10GENIChomozygous516576863
101288788912887890CA21GENIChomozygous519362224
101288821012888211TTACAC1GENIChomozygous689464616
101288872312888724TA43GENIChomozygous516576864
101288966612889667GC37GENICpossibly homozygous516576865
101288993512889936CG33GENIChomozygous516576866
101288995712889958TC30GENIChomozygous516576867
101289005012890051AG26GENIChomozygous516576868
101289122212891223TC28GENIChomozygous516576869