chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144942587144942588CT22GENIChomozygous115946160
7144944071144944072CT30GENIChomozygous115946162
7144944613144944614CT22GENIChomozygous115946163
7144944617144944618CT22GENIChomozygous115946165
7144944663144944664AG20GENIChomozygous115946167
7144945531144945532GT12GENIChomozygous115946171
7144945769144945770AG24GENIChomozygous115946173
7144945850144945851CT52GENIChomozygous115946175
7144947592144947593AC9GENIChomozygous115946177
7144947715144947716TG10GENIChomozygous115946181
7144951657144951658TC26GENICheterozygous115946185
7144951669144951670CT24GENICpossibly homozygous116378406
7144953087144953088TC19GENIChomozygous116378408
7144953638144953639CA15GENIChomozygous115946191
7144954758144954759GT16GENICpossibly homozygous115946195
7144954812144954813CT17GENICheterozygous116378410
7144955216144955217AG18GENIChomozygous116378412
7144961041144961042AG23GENIChomozygous115946205