chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6111477209111477210GC10GENIChomozygous886502018
6111477596111477597TG11GENIChomozygous886502019
6111477775111477776AG11GENIChomozygous886502020
6111477962111477963GC11GENIChomozygous886502021
6111478447111478448CT18GENIChomozygous886502022
6111478449111478450GA15GENIChomozygous886502023
6111478551111478552CT21GENIChomozygous886502024
6111478766111478767AG21GENIChomozygous886502025
6111478980111478981CT23GENIChomozygous886502026
6111479360111479361CT13GENIChomozygous886502027
6111479565111479566TA5GENIChomozygous886502028
6111479664111479665AG17GENIChomozygous886502029
6111479806111479807GA9GENIChomozygous886502030
6111480069111480070CT13GENIChomozygous886502031
6111480093111480094AG24GENIChomozygous886502032
6111480357111480358CT20GENIChomozygous886502033
6111480406111480407GA28GENIChomozygous886502034
6111480449111480450GA21GENIChomozygous886502035
6111480611111480612TC9GENIChomozygous886502036
6111480630111480631TC4GENIChomozygous886502037
6111480894111480895CT11GENIChomozygous886502038
6111481514111481515GA26GENIChomozygous886502039
6111481601111481602AG26GENIChomozygous886502040
6111482451111482452GA16GENICheterozygous886502041
6111482981111482982TC26GENIChomozygous886502042
6111483352111483353AG30GENIChomozygous886502043
6111483811111483812CT11GENIChomozygous886502044
6111484855111484856GA18GENIChomozygous886502045
6111485417111485418TC23GENIChomozygous886502046
6111485516111485517CT8GENIChomozygous886502047
6111485625111485626AC13GENIChomozygous886502048
6111485846111485847TC26GENIChomozygous886502049
6111486035111486036GA19GENIChomozygous886502050