chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69509690395096904TC20GENIChomozygous137852131
69509711795097118TG17GENIChomozygous137852132
69510118395101185AA14GENIChomozygous144749348
69510114995101150T14GENIChomozygous144749346
69510117895101179A14GENIChomozygous144749347
69510187095101871AG20GENIChomozygous137852134
69510224495102245AT17GENIChomozygous137852135
69510263495102634A14GENIChomozygous137698420
69510351695103517TC19GENIChomozygous137852137
69510399595103996GA11GENIChomozygous137852138
69510718895107189AG15GENIChomozygous137852139
69510731095107311AG12GENIChomozygous137852140
69511188095111881T20GENIChomozygous144749349
69511381795113818GC15GENIChomozygous137852142
69511619295116193AT25GENIChomozygous137852143
69511697295116973GT11GENIChomozygous137852144
69511822295118223T20GENIChomozygous137698423
69511862395118624AG21GENIChomozygous137852145
69511997895119979CA15GENIChomozygous137852146
69512003895120038A11GENIChomozygous137698424
69512086195120862TG21GENIChomozygous137852147
69512138295121383GA12GENIChomozygous137852148
69512243795122470CACACATCACCTCAGGCCTCTGGTACACTAGCG2GENIChomozygous137698425
69510283995102840CT18GENIChomozygous144769870
69510114995101150TA14GENICheterozygous403179722
69510115395101154T14GENICheterozygous403179723
69510115395101154TA14GENIChomozygous403179724
69511590995115910GC26GENIChomozygous144769872