chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124339161124339162GC18GENIChomozygous938508166
7124339853124339854CT16GENIChomozygous938508167
7124340150124340151TC20GENIChomozygous938508168
7124340593124340594GT37GENIChomozygous938508169
7124341640124341641CT28GENIChomozygous938508170
7124342221124342222AG21GENIChomozygous938508171
7124342808124342809AG35GENIChomozygous938508172
7124343070124343071TC24GENIChomozygous938508173
7124344290124344291CA24GENIChomozygous938508174
7124344725124344726AG13GENIChomozygous938508175
7124346017124346018AG30GENIChomozygous938508176
7124346085124346086CT28GENIChomozygous938508177
7124346457124346458AC23GENIChomozygous938508178
7124346977124346978TC24GENIChomozygous938508179
7124347350124347351CT19GENIChomozygous938508180
7124349089124349090TG14GENIChomozygous938508181
7124350157124350158GA19GENIChomozygous938508182
7124350303124350304TC22GENIChomozygous938508183
7124350783124350784CT14GENIChomozygous938508184
7124351259124351260TG18GENIChomozygous938508185
7124351260124351261GC19GENIChomozygous938508186
7124351265124351266AG16GENIChomozygous938508187
7124354044124354045TC15GENIChomozygous938508188
7124354543124354544TC24GENIChomozygous938508189
7124355098124355099CT22GENIChomozygous938508190
7124355645124355646GA17GENIChomozygous938508191
7124356412124356413AG17GENIChomozygous938508192
7124357561124357562GC23GENIChomozygous938508193
7124357590124357591CT24GENIChomozygous938508194
7124360268124360269GA15GENIChomozygous938508195
7124360930124360931GA22GENIChomozygous938508196
7124364056124364057CT22GENIChomozygous938508197
7124364485124364486GA14GENIChomozygous938508198
7124364758124364759CT15GENIChomozygous938508199
7124365980124365981CT22GENIChomozygous938508200
7124366145124366146TC21GENIChomozygous938508201
7124366572124366573GA26GENIChomozygous938508202