chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57618220676182207AG47GENIChomozygous113869748
57618258576182586CA34GENIChomozygous113869750
57618276176182761A31GENIChomozygous128199895
57618287676182877GA30GENIChomozygous113869752
57618297476182980GGGGGA22GENIChomozygous128199896
57618308476183085C34GENIChomozygous128199897
57618333176183332AG45GENIChomozygous113869754
57618338276183383TG36GENICpossibly homozygous113869756
57618345976183460CG35GENIChomozygous113869758
57618370976183720CCTGGGCAGTC41GENIChomozygous128199898
57618427676184276AA33GENICpossibly homozygous128199899
57618477576184776GA50GENIChomozygous113869762
57618479876184799AT48GENIChomozygous113869764
57618483776184838TC43GENIChomozygous113869766
57618608576186093CACTGTGT51GENIChomozygous128199900
57618621776186218GA39GENIChomozygous113869768
57618644776186448GT36GENIChomozygous113869770
57618644876186449AT36GENIChomozygous113869772
57618666576186666AG51GENIChomozygous113869774
57618724676187247TC50GENIChomozygous113869775