chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171307856713078568CT18GENIChomozygous111295544
171307935713079358GA30GENIChomozygous111295545
171308032313080324GA30GENIChomozygous111295546
171308073413080735CT25GENIChomozygous111295547
171308126113081262AT28GENIChomozygous111295548
171308128913081290AG28GENIChomozygous110962313
171308132913081330GA23GENIChomozygous111295549
171308145313081454AG17GENIChomozygous111295550
171308270513082706GA23GENIChomozygous111295551
171308367613083677GA24GENIChomozygous111295552
171308450013084501TA42GENIChomozygous111295553
171308479113084792TC42GENIChomozygous110962323
171308494913084950TC25GENIChomozygous110962325
171308508113085082CT34GENIChomozygous110962327
171308510213085103GA33GENIChomozygous111295554
171308510313085104TC33GENIChomozygous110962329
171308561813085619GA18GENIChomozygous110962331
171308604013086041TG16GENIChomozygous110962333
171308655513086556CG18GENIChomozygous111295555
171308661913086620AG21GENIChomozygous110962337
171308672413086725CG33GENIChomozygous110962339
171308681713086818CG29GENIChomozygous110962341
171308697313086974GA49GENIChomozygous111295556
171308715813087159CT32GENIChomozygous110962343
171308729013087291GA19GENIChomozygous111295557
171308750513087506TC21GENIChomozygous110962347