chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
165486220254862203AG16GENIChomozygous111827165
165486287254862873TG10GENIChomozygous111827167
165486355354863554GT11GENIChomozygous111827169
165486557654865577TC8GENIChomozygous111827171
165486562554865626CT15GENIChomozygous111827173
165486880554868806AG12GENIChomozygous111827175
165486979154869792CT13GENIChomozygous111827177
165486999254869993TG10GENIChomozygous111827179
165487074654870747CT14GENIChomozygous111827181
165487482654874827AG18GENIChomozygous111827183
165487596854875969AG10GENIChomozygous111827185
165487644754876448CT13GENIChomozygous111827187
165487677954876780TC8GENIChomozygous111827189
165487694754876948TC11GENIChomozygous111827191
165488769254887693GA16GENICheterozygous111827197
165489002954890030CT14GENIChomozygous111827199
165489244454892445AC28GENIChomozygous111827201
165489247554892476AG18GENIChomozygous111827203
165489524554895246CT15GENIChomozygous111827211
165489537554895376TC12GENIChomozygous111827213
165489634554896346TC20GENIChomozygous111827217
165489641954896420GT16GENIChomozygous111827219
165489666354896664TA18GENIChomozygous111827221
165489736354897364CA6GENIChomozygous111827223
165489390754893908CT5GENICheterozygous125664993