chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1670351137035114CT45GENIChomozygous111712254
1670355267035527AG41GENIChomozygous111712256
1670357677035770ACT43GENIChomozygous129330400
1670410987041099AT31GENIChomozygous111712258
1670416047041605GA25GENIChomozygous111712260
1670438887043889CG39GENIChomozygous111712262
1670456907045690C28GENIChomozygous129330401
1670456947045695TC31GENIChomozygous119093962
1670504217050422CT47GENICpossibly homozygous119093963
1670505517050552CT41GENICheterozygous119141635
1670534867053487AG52GENICpossibly homozygous119093966
1670552107055211CT29GENIChomozygous119093967
1670552157055216TC25GENIChomozygous119093968
1670552227055243AAAGGTAACCTAGGAGAAGGG23GENIChomozygous129330402
1670565747056575GA24GENIChomozygous111712264
1670575717057572TA41GENIChomozygous111712268
1670580387058038T39GENICpossibly homozygous129330403
1670586917058692AT42GENIChomozygous111712270
1670593717059372CT42GENIChomozygous111712272
1670603417060342AT42GENIChomozygous111712274
1670603627060363G34GENIChomozygous129330404
1670603647060367TAG34GENIChomozygous129330405
1670604637060463T20GENIChomozygous129330406
1670610987061099CT43GENIChomozygous111712276
1670621217062122CT45GENIChomozygous111712278
1670621947062195TC49GENIChomozygous111712280
1670631977063197ACAGAGAGAA34GENIChomozygous129330407
1670637507063753GTT33GENIChomozygous129330408
1670639727063973TC31GENIChomozygous111712283
1670667867066787CT37GENIChomozygous111712285
1670674427067443CT48GENIChomozygous111712287
1670679127067913T40GENIChomozygous129330409
1670733777073389ACCAACCAACCC5GENIChomozygous129330410
1670769287076956TCTCTCTCTCTCTCTGTGTGTGTGTGTG38GENICheterozygous129330411
1670770687077069CT49GENIChomozygous112219822
1670791057079106GA60GENIChomozygous111712289
1670796787079679GT48GENIChomozygous111712291
1670798927079898AATTTT52GENIChomozygous129330412
1670799797079979ACTCTG55GENIChomozygous129330413