chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67857186778571868AG26GENIChomozygous114866589
67859008678590087CA22GENIChomozygous115261400
67859321378593214TC17GENIChomozygous118554336
67859324578593246CG16GENIChomozygous114866599
67861532978615330CT15GENIChomozygous114866614
67861741278617413TC28GENIChomozygous118554337
67861741478617415GT28GENIChomozygous115261402
67868703078687031CA17GENIChomozygous115261406
67869789778697898CT17GENIChomozygous115261408
67870586378705864GA24GENIChomozygous114866797
67870587378705874CT21GENIChomozygous114866798
67870916378709164AT8GENIChomozygous115261410
67871153578711536GA15GENIChomozygous115261412
67871312378713124AC7GENIChomozygous115261414
67874840378748404GA13GENIChomozygous115261438
67874844278748443AT14GENIChomozygous114866949
67874846678748467GT14GENIChomozygous114866950
67875361878753619CT29GENIChomozygous115261442
67875385678753857GA45GENIChomozygous115261444
67875526678755267TC17GENIChomozygous114866981
67875760978757610CA23GENIChomozygous115261446
67875951678759517TC28GENIChomozygous114866989
67875957478759575GA29GENIChomozygous115261448
67875998478759985GA23GENIChomozygous115261450
67876189278761893AG18GENIChomozygous114866993
67876376678763767AG18GENIChomozygous114866996
67876616878766169TC25GENIChomozygous114866998
67877048978770490CG13GENIChomozygous115261452
67877281078772811GA30GENIChomozygous115261454
67877306978773070CT27GENIChomozygous115261456
67877307078773071CG27GENIChomozygous115261458
67877321678773217TA13GENIChomozygous115261460
67877379078773791GC21GENIChomozygous114867015
67877420378774204AG21GENIChomozygous115261462
67877421878774219CT19GENIChomozygous115261464
67877430478774305AT37GENIChomozygous118574285
67877430578774306GA37GENIChomozygous118574286
67877460578774606CT33GENIChomozygous114867017