chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
664553746455375AG7GENIChomozygous54286158
664555856455586A-4GENICheterozygous55402711
664556866455687AG9GENIChomozygous54286159
664559156455916TTG4GENIChomozygous54286160
664559376455938AG7GENIChomozygous54286161
664561186456119GA16GENICheterozygous54286162
664565206456521AT17GENICpossibly homozygous54286163
664568096456810TC15GENICpossibly homozygous54286164
664573776457378GGT1GENIChomozygous54286165
664575726457573AT9GENICpossibly homozygous54286166
664577106457711CG7GENICheterozygous54286167
664588646458865AG10GENICheterozygous54286174
664589866458987GC16GENICpossibly homozygous54286175
664591796459180AG12GENIChomozygous54286176
664592706459271CT9GENIChomozygous54286177
664596076459608AG14GENIChomozygous54286178
664613936461394CA4GENIChomozygous54286179
664618686461869GA11GENICheterozygous54286182
664620416462042GA12GENIChomozygous54286183
664623076462308AC10GENICpossibly homozygous54286184
664626986462699CT10GENICheterozygous54286186
664627556462756TA10GENICpossibly homozygous54286187
664631246463125GGA7GENIChomozygous54286189
664632486463249TC17GENIChomozygous54286190
664633676463368AG15GENICpossibly homozygous54286191
664635646463565CA5GENICheterozygous54286192
664635656463566CT5GENICheterozygous54286193
664638296463830CT14GENICpossibly homozygous54286194
664639136463914GA8GENIChomozygous54286195
664639336463934AG9GENICpossibly homozygous54286196
664640116464012GA2GENIChomozygous54286197
664640946464095AAC2GENIChomozygous54286198
664643856464386GA14GENICpossibly homozygous54286199
664645306464531TA10GENIChomozygous54286200
664646836464684TTCA10GENIChomozygous54286201
664647896464795CAGTAA------4GENIChomozygous54286202
664649446464945CT2GENIChomozygous54286203
664652006465201AG3GENIChomozygous54286204
664654946465495TA12GENICheterozygous54286205
664658106465811GT4GENIChomozygous54286206
664658516465852CT13GENIChomozygous54286207