chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67857186778571868AG21GENIChomozygous114866589
67859008678590087CA5GENIChomozygous115261400
67859324578593246CG11GENIChomozygous114866599
67861532978615330CT25GENIChomozygous114866614
67861741478617415GT20GENIChomozygous115261402
67859266878592669CT16GENIChomozygous118554335
67859321378593214TC10GENIChomozygous118554336
67861741278617413TC20GENIChomozygous118554337
67868703078687031CA15GENIChomozygous115261406
67870586378705864GA14GENIChomozygous114866797
67870587378705874CT12GENIChomozygous114866798
67870916378709164AT24GENICpossibly homozygous115261410
67871153578711536GA23GENIChomozygous115261412
67871312378713124AC27GENIChomozygous115261414
67875061878750619CA29GENIChomozygous114866966
67875233278752333AC25GENIChomozygous114866975
67875361878753619CT20GENIChomozygous115261442
67875385678753857GA15GENIChomozygous115261444
67875526678755267TC15GENIChomozygous114866981
67875760978757610CA18GENIChomozygous115261446
67875951678759517TC24GENIChomozygous114866989
67875957478759575GA17GENIChomozygous115261448
67875998478759985GA18GENIChomozygous115261450
67876189278761893AG17GENIChomozygous114866993
67876376678763767AG7GENIChomozygous114866996
67876616878766169TC22GENIChomozygous114866998
67877048978770490CG24GENIChomozygous115261452
67877281078772811GA19GENIChomozygous115261454
67877306978773070CT18GENIChomozygous115261456
67877307078773071CG18GENIChomozygous115261458
67877321678773217TA17GENIChomozygous115261460
67877379078773791GC19GENIChomozygous114867015
67877420378774204AG22GENIChomozygous115261462
67877421878774219CT22GENIChomozygous115261464
67877430478774305AT23GENIChomozygous118574285
67877430578774306GA25GENIChomozygous118574286
67877460578774606CT14GENIChomozygous114867017
67875480178754802GT18GENICheterozygous118641815