chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108774061887740619TC5GENIChomozygous68146157
108774072187740722AG2GENIChomozygous68146160
108774121587741216TC20GENIChomozygous68146162
108774146887741469CA15GENIChomozygous69718140
108774184787741848TC10GENIChomozygous68146165
108774208987742090TG24GENIChomozygous68146168
108774241887742419GA24GENIChomozygous68146171
108774326187743262GA9GENIChomozygous69718143
108774372287743723TC7GENIChomozygous68146174
108774438887744389TG8GENIChomozygous69718146
108774452487744525AG4GENIChomozygous68146177
108774465487744655CT10GENIChomozygous69718149
108774466587744666GT10GENIChomozygous69718152
108774491087744911AG16GENIChomozygous69718155
108774519887745199CT13GENIChomozygous69718157
108774574187745742TC14GENIChomozygous68146183
108774639787746398TC4GENIChomozygous68146186
108774676987746770TC14GENIChomozygous68146189
108774773187747732AT10GENIChomozygous69718160
108774920087749201GC5GENIChomozygous69718163
108774921187749212CT4GENIChomozygous69718166
108774955887749559GC5GENIChomozygous68146198
108774973887749739AC8GENIChomozygous69718172
108775035687750357CT12GENIChomozygous69718175
108775053887750539GA14GENIChomozygous69718178
108775099787750998CG7GENIChomozygous68146206
108775193587751936TC8GENIChomozygous69718181
108775238387752384TA6GENIChomozygous68146209
108775246887752469TC8GENIChomozygous68146212
108775285287752853GA12GENIChomozygous69718184