chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85090719550907196AG17GENIChomozygous138329605
85090775350907753C11GENIChomozygous138244842
85090853050908531AC19GENIChomozygous138329606
85091077050910771AG11GENIChomozygous138329607
85091093150910932AG11GENIChomozygous138329608
85091333550913340CTGGT10GENIChomozygous138244843
85091346850913469AT16GENIChomozygous138329610
85091348450913485GA16GENIChomozygous138329611
85091352350913530CTTTATC13GENIChomozygous138244844
85091469650914697GA14GENIChomozygous138329612
85091471750914718GA15GENIChomozygous138329613
85091666850916669A19GENIChomozygous138244845
85091704450917045CT13GENIChomozygous138329614
85091849250918493GA15GENIChomozygous138329615
85091883750918838CT21GENIChomozygous138329616
85092284350922844GA17GENIChomozygous138329617
85092286050922861AG16GENIChomozygous138329618
85092405050924056AGACAG9GENIChomozygous138244846
85092413650924140AGAC6GENIChomozygous142023731
85091616150916161AGA13GENICheterozygous148411097
85091918150919182CT11GENIChomozygous142070042
85092244550922446CT13GENIChomozygous142070043
85091989750919897CG9GENICpossibly homozygous142023729
85092401550924015CA12GENICpossibly homozygous142023730
85092460950924610GA11GENIChomozygous142070044
85092479450924796TT16GENIChomozygous138244847
85092546550925466AG15GENIChomozygous138329620
85092662150926622AG10GENIChomozygous142070045
85092709150927092AG16GENIChomozygous138329621
85092712350927124AG16GENIChomozygous138329622
85092811250928113CT8GENIChomozygous142070046
85092817550928176TC7GENIChomozygous138329623
85092849350928494AG12GENIChomozygous138329624
85092857150928572AC14GENIChomozygous138329625
85092858450928589AGGGC16GENIChomozygous138244848
85092949050929491CT9GENIChomozygous138329626
85093071750930718TC16GENIChomozygous138329627
85093097550930976CA9GENIChomozygous138329629