chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141327563141327564CT21GENIChomozygous115939902
7141328808141328809CT20GENIChomozygous115939903
7141329617141329618AG24GENIChomozygous115939904
7141330216141330217GA20GENIChomozygous115939905
7141334226141334227GA23GENIChomozygous115939910
7141334250141334251GT22GENIChomozygous115939911
7141335081141335082GC11GENIChomozygous115939912
7141335140141335141CT13GENIChomozygous115939913
7141336741141336742CT15GENIChomozygous115939914
7141338981141338982AG26GENIChomozygous115939915
7141340432141340433TC42GENIChomozygous115939917
7141341799141341800CT36GENIChomozygous115939918
7141342244141342245AG43GENIChomozygous115939919
7141342762141342763AG28GENIChomozygous115939920
7141342968141342969GT17GENIChomozygous115939921
7141344605141344606AG18GENIChomozygous115939924
7141345240141345241CT20GENIChomozygous115939925
7141345692141345693TG19GENIChomozygous115939926
7141347058141347059GA27GENIChomozygous115939927
7141349476141349477TC21GENIChomozygous115939928
7141351414141351415AC26GENIChomozygous115939929
7141353878141353879CT14GENIChomozygous115939930
7141354404141354405CT21GENICpossibly homozygous115939931
7141354506141354507AG20GENIChomozygous115939932