chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2218654673218654674AAGT18GENICpossibly homozygous60160718
2218654928218654929TC29GENIChomozygous59398955
2218655032218655033CT29GENIChomozygous60160719
2218656822218656823AG46GENIChomozygous59398958
2218657006218657007CCTG38GENIChomozygous59398961
2218657047218657077TGTGTGTGACTGTGTATGTGTGTGTGTATC------------------------------46GENIChomozygous60683597
2218657469218657470GA15GENIChomozygous60160723