chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34060178840601789AC29GENICheterozygous797878080
34060179440601795CT30GENICheterozygous797878081
34060180240601803CT28GENICheterozygous797878082
34060185240601853CT42GENICheterozygous797878083
34060185340601854CG41GENICheterozygous797878084
34060190740601908TC44GENICheterozygous797878085
34060192540601926TC52GENICheterozygous797878086
34060194640601947GA53GENICheterozygous797878087
34060194840601949GA49GENICheterozygous797878088
34060196140601962TC56GENICheterozygous797878089
34060197240601973CT57GENICheterozygous797878090
34060197740601978AG54GENICheterozygous797878091
34060198240601983GA54GENICheterozygous797878092
34060199340601994TC58GENICheterozygous797878093
34060199440601995GA57GENICheterozygous797878094
34060236040602361CT35GENIChomozygous797878095
34060260440602605AC35GENICpossibly homozygous797878096
34060266940602670GA29GENICheterozygous797878097
34060267940602680AG28GENICpossibly homozygous797878098
34060272440602725CG19GENICheterozygous797878099
34060277040602771CG17GENICpossibly homozygous797878100
34060278040602781AC21GENICpossibly homozygous797878101