chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113525116835251169GA71GENICheterozygous50729039
113525138535251386GA79GENIChomozygous50729040
113525359735253598GA36GENIChomozygous50729041
113525366335253664CCTG19GENIChomozygous50729042
113525417835254179TG60GENIChomozygous50729044
113525439335254394TC63GENIChomozygous50729045
113525480635254807CT56GENIChomozygous50729046
113525503735255038TTACACAC11GENICpossibly homozygous50729048
113525510435255105TC25GENIChomozygous50729049
113525567935255682TTG---51GENIChomozygous50729050
113525674335256746AAA---2GENIChomozygous50877697
113525884835258849GGA26GENIChomozygous50729051
113525886135258862TTA21GENIChomozygous50729052
113525971535259716TA54GENIChomozygous50729053
113525987435259875AAC38GENIChomozygous50729054
113525997735259978GGTT51GENIChomozygous50729055
113526064435260645GA55GENIChomozygous50729056
113526092635260932GTGTGT------4GENICheterozygous50729057
113526092835260932GTGT----4GENICheterozygous50729058
113526162935261630TA49GENIChomozygous50729059
113526185635261857GA54GENIChomozygous50729060
113526273935262740AT48GENIChomozygous50729061
113526334635263347GA60GENIChomozygous50729062
113526353335263534AT57GENIChomozygous50729063
113526368935263690GA40GENICpossibly homozygous50729064
113526378335263784TG40GENIChomozygous50729065
113526481035264811AC39GENIChomozygous50729066
113526541135265412GA61GENIChomozygous50729067
113526621235266216TTTT----7GENIChomozygous50729070
113526622435266225GA13GENICpossibly homozygous50729071
113526623635266237CT13GENIChomozygous50729072
113526623935266240GA12GENICpossibly homozygous50729073
113526625335266254GA14GENICpossibly homozygous50729074
113526625735266258GC15GENICpossibly homozygous50729075
113526632035266321G-25GENIChomozygous50729076
113526661135266612AG57GENIChomozygous50729077
113526816935268170TC43GENIChomozygous50729078