chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2096788139678814AG17GENIChomozygous45424330
2096797849679785CT16GENIChomozygous45424331
2096798819679882GA9GENIChomozygous45424332
2096800339680041AGAGAGAG--------4GENIChomozygous45424333
2096806459680646GA16GENIChomozygous45424334
2096817779681778CG25GENICheterozygous45424335
2096820629682063CT17GENICpossibly homozygous45424336
2096824849682485TC20GENIChomozygous45424337
2096829099682910AATT3GENIChomozygous45424338
2096829559682957CT--4GENIChomozygous45424339
2096836549683655TC5GENIChomozygous45424340
2096842759684276AG14GENICheterozygous45424345
2096845129684513CT21GENICpossibly homozygous45424346
2096850789685079CCT4GENIChomozygous45424347
2096852089685209AG19GENIChomozygous45424348
2096864479686448CT10GENIChomozygous45424349