chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148430823884308239AG15GENICpossibly homozygous113605611
148430826084308261TC15GENIChomozygous113605612
148430842784308428AG20GENIChomozygous113605613
148431009684310097AG20GENIChomozygous113605614
148431029884310299AG17GENIChomozygous113605615
148431045384310454AG33GENIChomozygous113605616
148431055084310551AG18GENIChomozygous113605617
148431083784310838GA16GENIChomozygous113605618
148431159884311599TA9GENIChomozygous113605619
148431177084311771TC15GENIChomozygous113605620
148431206084312061TC14GENICheterozygous113680107
148431206084312061TG14GENICheterozygous113680109
148431206484312065TC11GENICheterozygous113680111
148431217284312173TC23GENIChomozygous113605621
148431261084312611TC23GENIChomozygous113680113
148431354884313549AC9GENIChomozygous113605622
148431453284314533CG23GENIChomozygous113605623
148431470384314704CT16GENIChomozygous113605624
148431471184314712TC16GENIChomozygous113605625
148431475684314757TG19GENIChomozygous113605626
148431483684314837CT32GENIChomozygous113680115
148431501384315014AG32GENIChomozygous113605627
148431504784315048GT32GENIChomozygous113605628
148431544384315444TC30GENIChomozygous113605629
148431618884316189CG16GENIChomozygous113605630
148431632284316323GT19GENIChomozygous113605631
148431653084316531AG21GENIChomozygous113605632
148431677884316779TC22GENIChomozygous113605633
148431709184317092AG24GENIChomozygous113605634