chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122509539425095395TC20GENIChomozygous115485316
122509588225095883CA18GENIChomozygous115289613
122509624025096241C21GENIChomozygous128974057
122509692925096930TG12GENIChomozygous115289615
122509713625097137AG13GENIChomozygous115485318
122509748225097483TC13GENIChomozygous115289617
122509879525098796GA15GENIChomozygous115289621
122509889825098917TTTTTTTTTTGGGGGGGGG14GENIChomozygous128974060
122509902825099029GA8GENIChomozygous115485319
122509995025099950TTA12GENIChomozygous128974061
122510035525100356T11GENIChomozygous128974062
122510127525101276T16GENIChomozygous128974063
122510215925102160TC23GENIChomozygous115289631
122510262925102630GC17GENIChomozygous115289635
122510271525102716AG19GENIChomozygous115485320
122510275325102754TC18GENIChomozygous115289637
122510299025102991AG21GENIChomozygous115485321
122510322625103227GA8GENIChomozygous115485322
122510323525103240GGGGA7GENIChomozygous128974067
122509694825096949TG11GENIChomozygous118262439
122509696825096969TA12GENIChomozygous118262441
122509883025098831AG19GENIChomozygous115422806
122510464725104648TA8GENIChomozygous115422808
122510464925104650AC8GENIChomozygous115422810
122510115925101159TTT15GENICpossibly homozygous132892477
122510460025104604CTTT10GENIChomozygous132892478
122510552425105525TC26GENIChomozygous115289647
122510571425105715AG17GENIChomozygous115485323
122510599125105992TA31GENIChomozygous115289651
122510637025106371GA12GENIChomozygous115369124
122510663625106636AAAG10GENIChomozygous128974070
122510666525106666GA11GENIChomozygous115289657
122510667425106674GTGG10GENIChomozygous128974071
122510667825106679AG10GENIChomozygous115369126
122510706025107061TC23GENIChomozygous115485324
122510761325107614AG20GENIChomozygous115289665
122510776025107761TC14GENIChomozygous131916764
122510778025107781GA11GENIChomozygous118262442
122510801625108017TC15GENIChomozygous115485325