chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045935444593545CT18GENIChomozygous125226161
2045946674594668TC4GENIChomozygous125210019
2045949894594990CT11GENIChomozygous125226162
2045969834596984AC21GENIChomozygous125175932
2045981914598192TC9GENIChomozygous125175934
2045984264598427GT9GENIChomozygous125175937
2045984424598443GC7GENIChomozygous125175938
2045987274598728CT15GENIChomozygous125226164
2045987734598774GT26GENIChomozygous125226165
2045989464598947GA19GENIChomozygous125175939
2045990314599032CT28GENIChomozygous125226166
2045993424599343CT15GENIChomozygous125175941
2046011354601136CT21GENIChomozygous125226167
2046034094603410AC9GENIChomozygous125221331
2046035064603507GT13GENIChomozygous125175946
2046043104604311CT13GENICheterozygous125175949
2046043934604394AG4GENIChomozygous125175950
2046051994605200TG11GENIChomozygous125175952
2046054064605407AT30GENIChomozygous125199670
2046054784605479TA15GENIChomozygous125175953
2046057714605772CT7GENIChomozygous125175954
2046062504606251TC19GENIChomozygous125175955
2046068774606878GT20GENIChomozygous125175956
2046072504607251AC10GENIChomozygous125175957
2046074184607419GA16GENIChomozygous125175958
2046078324607833AC15GENIChomozygous125175960
2046079574607958AG23GENIChomozygous125175961
2046085754608576AC8GENIChomozygous125175962
2046085924608593TG8GENIChomozygous125175963
2046086044608605CA6GENIChomozygous125175964
2046086334608634AG12GENIChomozygous125175965
2046087544608755CT12GENIChomozygous125175966