chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160062808160062809CT43GENIChomozygous111791294
3160062838160062839T43GENIChomozygous127948160
3160064423160064424GT22GENIChomozygous111791296
3160065689160065690GT25GENIChomozygous111791298
3160065691160065692CT26GENIChomozygous111791300
3160065702160065703G25GENIChomozygous127948162
3160065712160065712G28GENIChomozygous127948163
3160065723160065723G29GENIChomozygous127948164
3160065742160065742G34GENIChomozygous127948165
3160065760160065761A37GENIChomozygous127948166
3160065765160065766C36GENIChomozygous127948167
3160065783160065786AAA33GENIChomozygous127948168
3160065789160065789G33GENIChomozygous127948169
3160065801160065801T33GENIChomozygous127948170
3160065811160065812CT36GENIChomozygous111791302
3160065825160065826C32GENIChomozygous127948171
3160065839160065840G37GENIChomozygous127948172
3160065843160065844GT38GENIChomozygous111791304
3160070823160070824A42GENIChomozygous127948174
3160070828160070829A42GENIChomozygous127948175
3160070896160070897A30GENIChomozygous127948176
3160070908160070909C32GENIChomozygous127948177
3160070913160070914A33GENIChomozygous127948178
3160070921160070922C36GENIChomozygous127948179
3160070925160070926C36GENIChomozygous127948180
3160078327160078327GT46GENICpossibly homozygous134674925