chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97114523471145235GGA4GENICheterozygous52411167
97114532571145326GA7GENIChomozygous52411168
97114731671147317CT15GENICheterozygous52411169
97114732071147321CT13GENICheterozygous52411170
97114733371147334C-12GENIChomozygous52411171
97114833371148334AC28GENIChomozygous52411172
97114927671149277AG16GENIChomozygous52411173
97115032471150325CG19GENIChomozygous52411174
97115120671151207AG22GENIChomozygous52411175
97115217771152181TTTT----7GENICheterozygous52411176
97115441271154413A-19GENIChomozygous52411177
97115578671155787AAGTGTGTGT7GENIChomozygous52411178
97115633971156340AG21GENIChomozygous52411179
97115691271156913CCA7GENICheterozygous52411180
97115777471157775CA20GENIChomozygous52411181
97115879471158795TG30GENIChomozygous52411182
97116100871161009CT15GENIChomozygous52411183
97116655971166560T-3GENIChomozygous52411186
97115249371152494TG29GENICheterozygous52473107
97116283271162833GGT23GENIChomozygous52013356
97116134271161343CT24GENIChomozygous52411184
97116634871166349TC11GENIChomozygous52411185
97116660771166608AG14GENICheterozygous52411187
97116784371167844AG31GENIChomozygous52411188
97116790571167906TC19GENIChomozygous52411189
97116852471168525GA22GENIChomozygous52411190
97117043471170435GGAA17GENICpossibly homozygous52411191
97117051271170513TTAA16GENIChomozygous52013357
97117066771170668GGT16GENIChomozygous52013358
97117106371171064AG24GENIChomozygous52411192
97117254571172576AGCTCTCTTGAGGGCTTTTCATATTAGAACG-------------------------------7GENIChomozygous52411193
97117409371174094TTC6GENIChomozygous52411194
97117630471176305AAACAC9GENICheterozygous52013360
97117630771176309AC--9GENICpossibly homozygous52411195
97117780971177810T-15GENIChomozygous52013361
97117781471177815T-14GENIChomozygous52013362
97117017471170175T-15GENICheterozygous52233637