chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71265310912653110GT11GENIChomozygous115570305
71265336312653364CT21GENIChomozygous115570306
71265343212653433AT19GENIChomozygous115570307
71265382012653820G13GENIChomozygous128435832
71265384812653849GA13GENIChomozygous115570308
71265501612655017TG26GENICpossibly homozygous115570309
71265549712655498C28GENIChomozygous128435833
71265622812656229TC23GENIChomozygous115570310
71265726512657266C18GENIChomozygous128435834
71265726712657270TTC18GENIChomozygous128435835
71265728412657284T17GENIChomozygous128435836
71265765612657657GA6GENIChomozygous115570312
71265768312657684CG13GENICheterozygous118251054
71265876212658762GGGCCTTGCGCTTCCTAG5GENIChomozygous128435837
71265897012658971GA27GENIChomozygous115570313
71265936312659364C12GENICheterozygous128435838
71265970312659704TC15GENIChomozygous115570315
71266022412660225TC11GENIChomozygous115570316
71266024312660244AG10GENIChomozygous115570317
71266113212661133CT21GENIChomozygous115570318
71266246612662467GA26GENIChomozygous115570323
71266127012661271AG19GENIChomozygous115570319
71266216912662170AT18GENIChomozygous115570320
71266244512662446TC27GENIChomozygous115570322
71266251012662511CG25GENIChomozygous115570324
71266377512663775G22GENIChomozygous128435839