chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2247189515247189516TC29GENIChomozygous110363446
2247189601247189602AC27GENICpossibly homozygous110363448
2247189652247189653GA27GENIChomozygous110363450
2247189837247189838AG32GENIChomozygous110363452
2247190870247190871CG34GENIChomozygous110363456
2247190984247190985GA33GENIChomozygous110363458
2247191184247191185CT29GENIChomozygous110363460
2247191194247191195AT29GENIChomozygous111193366
2247191262247191263TC27GENIChomozygous110363462
2247191442247191443TA27GENIChomozygous111388809
2247191453247191454CT30GENIChomozygous111388811
2247192072247192073CA24GENIChomozygous110363466
2247192105247192106GA14GENIChomozygous110363468
2247192519247192520AT32GENIChomozygous110363472
2247192894247192895CT31GENIChomozygous110363474
2247192912247192913TG30GENIChomozygous110363478
2247192966247192967GA27GENIChomozygous110363480
2247193150247193151AT16GENIChomozygous110363482
2247193170247193171CT20GENIChomozygous110363484
2247193221247193222AG23GENIChomozygous111193370
2247193705247193706AG29GENIChomozygous111193372
2247194358247194359GT15GENIChomozygous111193374
2247194399247194400CA16GENIChomozygous111193376
2247195027247195028TC28GENIChomozygous110363490
2247195304247195305CT40GENICpossibly homozygous111193378
2247196978247196979CA21GENIChomozygous110363492