chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107469813974698140CT22GENIChomozygous117064990
107470102274701023CA18GENIChomozygous117064994
107470619774706198AT16GENIChomozygous117064998
107470650974706510TC26GENIChomozygous117065000
107470651474706515GA26GENIChomozygous117065002
107470814674708147AT11GENIChomozygous116637544
107470959774709598AG17GENIChomozygous116637546
107470995874709959GA20GENIChomozygous116637548
107471044474710445GA30GENIChomozygous116637550
107471086374710864TC14GENIChomozygous116637554
107471117474711175AC15GENIChomozygous116637556
107471259674712597GC26GENIChomozygous116637558
107471338474713385AG15GENIChomozygous116637560
107471389274713893GT27GENIChomozygous116637562
107471505174715052GA12GENIChomozygous116637564
107471701874717019GA10GENIChomozygous117065008
107471872774718728CA30GENIChomozygous117065010
107471881574718816TC29GENIChomozygous116637572
107471893174718932AG19GENIChomozygous117065012
107471967874719679TA19GENIChomozygous116637574
107472011174720112TC16GENIChomozygous116637576