chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108774061887740619TC31GENIChomozygous68146157
108774072187740722AG31GENIChomozygous68146160
108774121587741216TC54GENIChomozygous68146162
108774184787741848TC48GENIChomozygous68146165
108774208987742090TG52GENIChomozygous68146168
108774241887742419GA71GENIChomozygous68146171
108774372287743723TC45GENIChomozygous68146174
108774452487744525AG37GENIChomozygous68146177
108774491287744913GA63GENIChomozygous68146180
108774574187745742TC36GENIChomozygous68146183
108774639787746398TC53GENIChomozygous68146186
108774676987746770TC55GENIChomozygous68146189
108774808587748086CT48GENIChomozygous68146192
108774860887748609TG18GENIChomozygous68146195
108774955887749559GC53GENIChomozygous68146198
108774960187749602GA43GENICpossibly homozygous68146201
108775075487750755GA48GENIChomozygous68146204
108775099787750998CG33GENIChomozygous68146206
108775238387752384TA48GENIChomozygous68146209
108775246887752469TC43GENIChomozygous68146212