chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139909227599092275T38GENIChomozygous131136043
139909285399092853CTT72GENIChomozygous131136044
139909328299093283CT56GENIChomozygous114651306
139909411699094116C58GENIChomozygous131136045
139909493499094934TCT59GENIChomozygous131136046
139909501299095013AG51GENIChomozygous118547983
139909501799095018AT50GENIChomozygous118547984
139909501999095020AT52GENIChomozygous118547985
139909616799096168AG59GENIChomozygous118547986
139909631999096319A50GENIChomozygous131136047
139909640299096402AACTATGTACTTTAAAGAAAAGATGAATTTTT46GENIChomozygous131136048
139909832799098328AC28GENIChomozygous118547988
139909836699098367AG36GENIChomozygous126105640
139909881199098812GA59GENIChomozygous114651308
139909969399099694AG69GENIChomozygous118547989
139910130199101302AC35GENIChomozygous114651310
139910168299101682TTGGA64GENICpossibly homozygous131136050
139909517399095174CT42GENIChomozygous114437294
139909517699095177CT42GENIChomozygous114437296
139909519099095191GC42GENIChomozygous114437298
139909526599095266GA63GENIChomozygous114437300
139909973599099736TC68GENIChomozygous131140618