chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
26092907060929071AT29GENIChomozygous602969941
26092908660929087TC28GENIChomozygous602969942
26092921160929212TTTA17GENICpossibly homozygous730460399
26092926560929266TG38GENIChomozygous602969943
26092988660929887TC32GENIChomozygous601700294
26093054760930548AG27GENIChomozygous601700295
26093071960930720GA23GENIChomozygous601700296
26093085860930859AG29GENIChomozygous601700297
26093121160931212AT36GENIChomozygous601700298
26093174360931744TA29GENIChomozygous601700299
26093189860931899TC30GENIChomozygous601700300
26093212160932122TA38GENIChomozygous601700301
26093218360932184AG38GENIChomozygous601700302
26093268960932690CT32GENIChomozygous601700303
26093270360932704AG32GENIChomozygous601700304
26093300360933004AAACACACACAC10GENIChomozygous730460400
26093303260933033GA16GENIChomozygous601700305
26093303960933040AAACACAC18GENIChomozygous730460402
26093311160933112AC20GENIChomozygous601700306
26093325960933260CT24GENIChomozygous601700307