chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100837186100837187CG29GENIChomozygous109563190
1100837279100837280TC36GENIChomozygous109563191
1100837873100837874TC40GENIChomozygous109563192
1100839112100839113GA38GENIChomozygous109563193
1100841162100841163AG31GENIChomozygous109563194
1100841605100841606TC32GENIChomozygous109563195
1100843980100843981AC14GENICpossibly homozygous109563196