chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108685257386852574CT29GENIChomozygous51528990
108685394486853945GT51GENIChomozygous51528991
108685436186854363GA--42GENIChomozygous51528992
108685490086854901AT36GENIChomozygous51528993
108685517286855173CT44GENIChomozygous51528994
108685567186855672GA48GENIChomozygous51528995
108685621286856213TG50GENIChomozygous51528996
108685678686856787C-28GENIChomozygous51528997
108685783686857837CT44GENIChomozygous51528998
108685824786858248AC59GENICpossibly homozygous51528999
108685833986858340GT48GENIChomozygous51529000
108685945986859460AAC7GENIChomozygous51529001