chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103634554136345542TC5INTERGENIChomozygous51413697
103634554836345549AAGGTGATGGGGGAAACTGAGAAAAGCCAACT7INTERGENIChomozygous52316258
103634580536345806TG18INTERGENIChomozygous51413699
103634609636346097CA28INTERGENIChomozygous51413701
103634632636346330AAAA----19INTERGENIChomozygous51413703
103634641336346414CT22INTERGENIChomozygous51413705
103634700836347009CT26INTERGENIChomozygous51413707
103634798136347982AG15INTERGENIChomozygous51413709
103634837436348375TTC18INTERGENIChomozygous51413711
103634853236348533G-15INTERGENIChomozygous51413713
103634862736348628TC23INTERGENIChomozygous51413715
103634937436349375AG9INTERGENIChomozygous51413717
103635004636350047TC29INTERGENIChomozygous51413719
103635005036350051GA26INTERGENIChomozygous51413721
103635207336352074TC12INTERGENIChomozygous51413723
103635219736352198CT20INTERGENIChomozygous51413725
103635223536352236CT23INTERGENIChomozygous51413727
103635224936352250TC24INTERGENIChomozygous51413729
103635233736352338AG26INTERGENIChomozygous51413731
103635258036352581GGA16INTERGENIChomozygous51413733
103635281036352811CT21INTERGENIChomozygous51413735
103635311536353116AG29INTERGENIChomozygous51413737
103635382436353825CT21INTERGENIChomozygous51413739
103635390536353906TC34INTERGENIChomozygous51413741
103635407436354075GA23INTERGENIChomozygous51413743
103635440136354406ACATT-----17INTERGENIChomozygous52316259
103635460936354610AC14INTERGENIChomozygous51413751
103635491236354913AT13INTERGENIChomozygous51413753
103635514936355150AG12INTERGENIChomozygous51413755
103635528936355290AAG12INTERGENIChomozygous51413757
103635533336355334CT19INTERGENIChomozygous51413759
103635540536355406TA16INTERGENIChomozygous51413761
103635665236356653TG33INTERGENIChomozygous51413766
103635679036356791T-23INTERGENICheterozygous51413768
103635726836357269AAGAGAGAGAGAGAGAGG17GENIChomozygous52316260
103635728936357290GA27GENIChomozygous51413770
103635738636357387AG22GENIChomozygous51413772
103635757136357572CT37GENIChomozygous51413774
103635778636357787TC19GENIChomozygous51413776
103635779536357796TC21GENIChomozygous51413778
103635860836358611AAG---26GENIChomozygous51413780
103635885236358853AG30GENIChomozygous51413782
103635901036359018CTGGGCTA--------30GENIChomozygous51413784
103635934136359342GA30GENIChomozygous51413786
103636008236360083AATG27GENICpossibly homozygous51413788
103636096336360964AG22GENIChomozygous51413790
103636117136361172GA32GENIChomozygous51413792
103635441836354426ACACACAC--------8INTERGENICheterozygous52367872
103635442036354426ACACAC------8INTERGENICpossibly homozygous52367874