chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18916285489162855AG43GENIChomozygous977873167
18916353489163535TC91GENIChomozygous977873168
18916399789163998GA50GENIChomozygous977873169
18916457589164576GA27GENIChomozygous977873170
18916460189164602TC22GENIChomozygous977873171
18916471989164720TC13GENIChomozygous977873172
18916476089164761CA29GENICpossibly homozygous977873173
18916530789165308TC48GENIChomozygous977873174
18916634589166346CT47GENIChomozygous977873175
18916721689167217AT68GENIChomozygous977873176
18916760989167610CT47GENIChomozygous977873177
18916824489168245GA52GENIChomozygous977873178
18916825489168255TC51GENIChomozygous977873179
18916826489168265GT48GENIChomozygous977873180
18916827789168278CT48GENIChomozygous977873181
18916833889168339AG37GENIChomozygous977873182
18916838089168381AG33GENIChomozygous977873183
18916842589168426GT30GENIChomozygous977873184
18916899889168999AG49GENIChomozygous977873185
18916920589169206AC38GENIChomozygous977873186
18916981889169819CT41GENIChomozygous977873187
18917020589170206AG66GENIChomozygous977873188
18917090289170903AG37GENIChomozygous977873189
18917178289171783CT30GENIChomozygous977873190
18917239189172392GA32GENIChomozygous977873191
18917313189173132CT60GENIChomozygous977873192
18917324089173241TA88GENIChomozygous977873193
18917379689173797AG34GENIChomozygous977873194
18917415189174152AT33GENIChomozygous977873195
18917415889174159TC41GENIChomozygous977873196
18917417689174177CA43GENIChomozygous977873197
18917429889174299CT49GENIChomozygous977873198
18917434189174342GA34GENIChomozygous977873199
18917439089174391TC28GENIChomozygous977873200
18917451989174520TC60GENIChomozygous977873201
18917542289175423AT56GENIChomozygous977873202