chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165716419165716420GA13GENIChomozygous111809954
3165716460165716461AG19GENIChomozygous111809956
3165716510165716511GT21GENIChomozygous111809958
3165716853165716854AG11GENIChomozygous111809961
3165717505165717506GA6GENIChomozygous111809963
3165718421165718422AT10GENIChomozygous111809965
3165718770165718771TC18GENIChomozygous111809968
3165719406165719407GA5GENIChomozygous112045973
3165719864165719865CT17GENIChomozygous111809970
3165720755165720756TC5GENIChomozygous111809973
3165721423165721424GA11GENIChomozygous111809975
3165722683165722684TG3GENICheterozygous125869865
3165723500165723501AG8GENIChomozygous111809977
3165724937165724938CG18GENIChomozygous111809979
3165725666165725667CG14GENIChomozygous111809987
3165725787165725788GA12GENIChomozygous111809989
3165727125165727126GA20GENIChomozygous111810001
3165727365165727366TC14GENIChomozygous111810003
3165729494165729495AG7GENIChomozygous111810005
3165729803165729804CG14GENIChomozygous111810008
3165730403165730404GA20GENIChomozygous111810010
3165730805165730806CT8GENIChomozygous111810012
3165732005165732006GT4GENIChomozygous125869866
3165732006165732007GT4GENIChomozygous125869867
3165732815165732816TC6GENIChomozygous111810017
3165733239165733240AG12GENIChomozygous111810019
3165733902165733903AG14GENIChomozygous111810022
3165734051165734052CT12GENIChomozygous111810024
3165734529165734530GA22GENICheterozygous111810027
3165734668165734669AG24GENIChomozygous111810029
3165734746165734747AG12GENICheterozygous111810032
3165734887165734888GA22GENIChomozygous111810034
3165735012165735013CG17GENIChomozygous111810036
3165736652165736653GA20GENIChomozygous111810039
3165740269165740270CT4GENIChomozygous111810043
3165740601165740602CT21GENIChomozygous111810046
3165740912165740913GA20GENIChomozygous111810048