chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2091029609102961AG37GENIChomozygous45679192
2091030529103056GGAA----30GENIChomozygous45679193
2091035589103559AG19GENIChomozygous45679194
2091036349103635CA20GENIChomozygous45679195
2091036379103638CA20GENIChomozygous45679196
2091036659103666GGT15GENIChomozygous45421602
2091037169103717TC14GENIChomozygous45679197
2091037419103742A-4GENIChomozygous45679198
2091037489103749AAT11GENICheterozygous45421606
2091037489103749AATAT11GENICpossibly homozygous45679199
2091038799103880AT18GENIChomozygous45679200
2091044729104473G-11GENIChomozygous45421608
2091044829104483T-7GENIChomozygous45421610
2091044859104486A-7GENIChomozygous45421612
2091044919104492A-7GENIChomozygous45421613
2091045019104502G-9GENIChomozygous45421615