chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19416740294167403AG6GENIChomozygous141219050
19416763594167635TTAG14GENIChomozygous141163360
19416780894167809GA18GENIChomozygous141219051
19417015294170153AG16GENIChomozygous141219056
19416917794169178TC15GENIChomozygous141219052
19416989294169893GT25GENIChomozygous141219054
19417004994170050GT12GENIChomozygous141219055
19417067994170680CT16GENIChomozygous141219057
19417083994170840AG30GENIChomozygous141219058
19417103694171037CT19GENIChomozygous141219059
19417116394171164TC27GENIChomozygous141219060
19417166294171663AG18GENIChomozygous141219061
19417267294172673GC3GENIChomozygous141219062
19417496594174966GA16GENIChomozygous141219068
19417324894173249AG13GENIChomozygous141219063
19417335794173358AG12GENIChomozygous141219064
19417342094173421GA13GENIChomozygous141219065
19417427294174273CA21GENIChomozygous141219066
19417464094174641AG16GENIChomozygous141219067
19417267494172675GC3GENIChomozygous145283488
19417506394175064CA12GENIChomozygous141219069
19417507994175080AG9GENIChomozygous141219070
19417517994175180GC21GENIChomozygous141219071
19417595394175954TG30GENIChomozygous141219072
19417651994176520CT27GENIChomozygous145283489
19417668594176686GA18GENIChomozygous141219073
19417674194176742TC15GENIChomozygous141219074
19417678394176784TC16GENICpossibly homozygous141219075
19417568794175688A14GENICheterozygous403795113
19417568794175688AG14GENIChomozygous403795114