chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227050902227050903AT23GENIChomozygous108998650
1227051528227051529CT29GENIChomozygous109198469
1227052289227052290AG30GENIChomozygous108998652
1227054520227054521GA26GENIChomozygous109198471
1227054820227054821TC31GENIChomozygous108998653
1227054999227055000TC17GENIChomozygous109198473
1227055892227055893AG21GENIChomozygous109198475
1227056123227056124AG12GENIChomozygous109198477
1227056962227056963CT24GENIChomozygous109198479
1227057742227057743TA28GENIChomozygous109198481
1227057970227057971CT26GENIChomozygous109198483
1227059441227059442AG23GENIChomozygous109198485
1227059522227059523TC20GENIChomozygous109198487
1227059800227059801TC22GENIChomozygous108998656
1227060073227060074CT22GENIChomozygous108998657
1227060155227060156GT9GENIChomozygous108998658
1227060662227060663TC34GENIChomozygous108998659
1227060834227060835CA29GENIChomozygous109198489
1227061068227061069CA15GENIChomozygous109198491
1227061708227061709CT10GENIChomozygous109198493
1227063341227063342CT27GENIChomozygous109198495
1227064245227064246AG26GENIChomozygous108998660
1227065989227065990AG15GENIChomozygous109198497
1227067067227067068TA26GENIChomozygous109198499
1227067549227067550GA24GENIChomozygous109198501
1227068931227068932TG12GENIChomozygous109198503
1227069559227069560AG15GENIChomozygous108998665