chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143260605143260606A-2GENIChomozygous55759107
5143261105143261106CT12GENIChomozygous55759108
5143261652143261654GT--13GENIChomozygous56355253
5143261655143261669TGCAGGTATACAGG--------------14GENIChomozygous56355254
5143262275143262276AG13GENICpossibly homozygous55759111
5143262438143262439GA3GENICheterozygous55759112
5143263477143263484TAGTACA-------1GENIChomozygous56355256
5143263545143263546GT11GENICpossibly homozygous55759117
5143264377143264378GC13GENICpossibly homozygous55759118
5143266675143266676CG15GENIChomozygous55759119
5143273181143273182AG8GENIChomozygous55759124
5143273354143273355CCCT4GENIChomozygous55759125
5143275031143275032GA14GENIChomozygous55759126
5143277873143277874AG14GENICpossibly homozygous55759130
5143278412143278413CT1GENIChomozygous55759132
5143278583143278584AAT11GENIChomozygous55759133
5143279644143279645TC17GENIChomozygous55759134
5143283394143283401TTCAACC-------2GENIChomozygous55759136
5143284462143284463GGAAA5GENICheterozygous56067637
5143285526143285527TG11GENIChomozygous55759142
5143286150143286151TC19GENIChomozygous55759143
5143286826143286827GT4GENICheterozygous55759150
5143287079143287080GT17GENIChomozygous55759151
5143287158143287159AG13GENICpossibly homozygous55759152
5143287295143287296CT14GENICpossibly homozygous55759153
5143287910143287911TC1GENIChomozygous55759158