chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113525116835251169GA25GENICheterozygous50729039
113525138535251386GA20GENIChomozygous50729040
113525359735253598GA24GENIChomozygous50729041
113525366335253664CCTG14GENICpossibly homozygous50729042
113525417835254179TG23GENIChomozygous50729044
113525439335254394TC23GENIChomozygous50729045
113525480635254807CT22GENIChomozygous50729046
113525503735255038TC42GENICheterozygous50729047
113525503735255038TTACACAC14GENIChomozygous50729048
113525510435255105TC26GENIChomozygous50729049
113525567935255682TTG---26GENIChomozygous50729050
113525884835258849GGA1GENIChomozygous50729051
113525886135258862TTA1GENIChomozygous50729052
113525971535259716TA41GENIChomozygous50729053
113526092635260932GTGTGT------13GENICheterozygous50729057
113525987435259875AAC18GENIChomozygous50729054
113525997735259978GGTT5GENIChomozygous50729055
113526064435260645GA30GENIChomozygous50729056
113526092835260932GTGT----13GENICheterozygous50729058
113526162935261630TA29GENIChomozygous50729059
113526185635261857GA34GENIChomozygous50729060
113526273935262740AT37GENIChomozygous50729061
113526334635263347GA25GENIChomozygous50729062
113526353335263534AT32GENICpossibly homozygous50729063
113526368935263690GA19GENIChomozygous50729064
113526378335263784TG28GENIChomozygous50729065
113526481035264811AC33GENIChomozygous50729066
113526541135265412GA49GENIChomozygous50729067
113526621235266216TTTT----6GENIChomozygous50729070
113526622435266225GA11GENICpossibly homozygous50729071
113526623635266237CT11GENICpossibly homozygous50729072
113526623935266240GA12GENIChomozygous50729073
113526625335266254GA13GENICheterozygous50729074
113526625735266258GC15GENICpossibly homozygous50729075
113526632035266321G-26GENIChomozygous50729076
113526661135266612AG38GENIChomozygous50729077
113526816935268170TC24GENIChomozygous50729078