chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104363293443632935CT18GENIChomozygous116578973
104363303043633031GA24GENIChomozygous116578975
104363445243634453TG16GENIChomozygous116578977
104363502343635024CA19GENIChomozygous116578979
104363514543635146AG20GENIChomozygous116578981
104363520643635207AG17GENIChomozygous116578983
104363527543635276GA16GENIChomozygous116578985
104363536643635367CT14GENIChomozygous116578987
104363544943635450GT13GENIChomozygous116578989
104363553843635539CT17GENIChomozygous116578991
104363556243635563CT21GENIChomozygous116578993
104363557043635571GC23GENIChomozygous116578995
104363559543635596AT18GENIChomozygous116578997
104363575143635752GA13GENIChomozygous116578999
104363577943635780AG13GENIChomozygous116579001
104363594043635941CT3GENIChomozygous116579003
104363595443635955AG2GENIChomozygous116579005
104363616443636165CG17GENIChomozygous116579009
104363620143636202AT15GENIChomozygous116579011
104363625543636256GA12GENIChomozygous116579013
104363681343636814AG14GENIChomozygous116579017
104363696643636967TC20GENIChomozygous116579019
104363702543637026CT27GENIChomozygous116579021
104363705643637057GA25GENIChomozygous116579023
104363723343637234CT11GENIChomozygous116579025
104363726643637267CT11GENIChomozygous116579027
104363729943637300CT17GENIChomozygous116579029
104363801943638020GA18GENIChomozygous116579031
104363833143638332AG14GENIChomozygous116579033
104363842343638424CG16GENIChomozygous116579035
104363869043638691TC11GENIChomozygous116579037
104363877943638780CT15GENIChomozygous116579039
104363892543638926GA11GENIChomozygous116579041