chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108803879588038796CT67GENIChomozygous52205537
108803894888038949C-3GENIChomozygous51534190
108803897688038977AG27GENIChomozygous51534191
108803900688039007CG13GENIChomozygous51534192
108803906488039065A-2GENIChomozygous52650767
108803945788039458AG22GENIChomozygous51534193
108804009888040099AT10GENIChomozygous51534197
108804009988040100AT10GENIChomozygous53378393
108804026188040262T-30GENIChomozygous51534198
108804033988040340TC61GENIChomozygous51534199
108804036788040368CT68GENICpossibly homozygous51534200
108804045388040454AT18GENIChomozygous51534201
108804011188040112CT15GENIChomozygous53378395
108804014988040150AG24GENIChomozygous53378397
108804059788040598TTTGTGTGTGTGTGTGTGTGTGTGTG20GENIChomozygous52507564