chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185464834954648350G14GENIChomozygous140225312
185465037554650376CT18GENIChomozygous140325195
185465039954650400GA21GENIChomozygous140325196
185465040054650401CA21GENIChomozygous140325197
185465053454650535AG17GENIChomozygous140325198
185465072554650725A22GENIChomozygous140225315
185465084354650844TC16GENIChomozygous140325199
185465120354651203AA18GENIChomozygous140225316
185465130354651304AG20GENIChomozygous140325202
185464949454649495GA30GENIChomozygous146304214
185465095954650960GA14GENIChomozygous146304215
185465132054651321AT20GENIChomozygous146304216
185465177354651774AC22GENIChomozygous140325203
185465200754652008AC23GENIChomozygous140325204
185465299054652991AG20GENIChomozygous140325206
185465476254654763GA20GENIChomozygous140325207
185465559454655595GC26GENIChomozygous140325208
185465757154657572TC22GENIChomozygous140325209
185465887754658878CT26GENIChomozygous140325210
185466217954662180TC20GENIChomozygous140325211
185466488954664896GTGTGTG10GENIChomozygous140225317
185466565954665660AG8GENIChomozygous146304217
185466567954665680CA14GENIChomozygous146304218
185466609754666098GA20GENIChomozygous146304219
185466617254666173TC23GENIChomozygous140325213
185466647054666471CT12GENIChomozygous146304220