chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2096788139678814AG27GENIChomozygous45424330
2096797849679785CT54GENIChomozygous45424331
2096798819679882GA48GENICpossibly homozygous45424332
2096800339680041AGAGAGAG--------35GENIChomozygous45424333
2096806459680646GA59GENICpossibly homozygous45424334
2096817779681778CG38GENIChomozygous45424335
2096820629682063CT60GENIChomozygous45424336
2096824849682485TC51GENIChomozygous45424337
2096829099682910AATT23GENIChomozygous45424338
2096829559682957CT--19GENIChomozygous45424339
2096836549683655TC33GENICpossibly homozygous45424340
2096840299684031AG--15GENICheterozygous45424341
2096840349684035AAG18GENICheterozygous45424342
2096840379684038AAAG19GENICheterozygous45424343
2096840429684043G-17GENICheterozygous45424344
2096842759684276AG52GENIChomozygous45424345
2096845129684513CT63GENIChomozygous45424346
2096850789685079CCT37GENIChomozygous45424347
2096852089685209AG48GENIChomozygous45424348
2096864479686448CT29GENIChomozygous45424349