chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144612596144612597TG13GENIChomozygous115945535
7144612831144612832TA16GENIChomozygous115945536
7144612872144612872TA15GENICpossibly homozygous128531960
7144613211144613212TC16GENIChomozygous115945539
7144615862144615863TC18GENIChomozygous115945541
7144616807144616808AT24GENIChomozygous115945542
7144617662144617663CT19GENIChomozygous115945547
7144623071144623072CT21GENIChomozygous115945549
7144624424144624425TG19GENIChomozygous115945550
7144624749144624750AC17GENIChomozygous115945552
7144625439144625440GA20GENIChomozygous115945553
7144625693144625694CA13GENIChomozygous115945555
7144621755144621756TC19GENIChomozygous118515938
7144620316144620316T9GENIChomozygous135187431
7144620776144620776A22GENICpossibly homozygous129940159