chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142049420520494206GA37GENICpossibly homozygous139472289
142049428320494284GA42GENIChomozygous139472290
142049484920494850TC42GENIChomozygous139472291
142049515820495159CG39GENIChomozygous139472292
142049672620496730ACAC34GENIChomozygous139384085
142049754220497543TC30GENIChomozygous139472293
142049817420498175CT41GENIChomozygous139472294
142049998620499987GA48GENICpossibly homozygous139472295
142050024220500243TC53GENIChomozygous139472296
142050188420501885C22GENIChomozygous139384086
142050208920502090TA34GENIChomozygous139472297
142050255920502560AG41GENIChomozygous139472298
142050264020502641GA41GENIChomozygous139472299