chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105946678359466784T-19GENICpossibly homozygous51897669
105946797359468001AGAGAGAGAGAGAGAGAGAGAGAGAGAG----------------------------5GENIChomozygous52379090
105947223259472233CG42GENIChomozygous51465616
105947225459472255GA35GENIChomozygous51897689
105947229959472300CT19GENIChomozygous51897691
105947261459472624CCAAACCAAA----------5GENIChomozygous52460861
105947296259472963AG38GENIChomozygous52062257
105946825859468259GA19GENIChomozygous52062253
105947281759472818TC37GENIChomozygous52062255
105947323759473238TC48GENIChomozygous52062259
105947413659474137TA38GENICpossibly homozygous52062261
105947452359474524GA43GENIChomozygous52062263
105947471759474718AG47GENIChomozygous52062265
105947475359474754GA44GENIChomozygous52062267
105947512459475125AC30GENIChomozygous52062269
105947539159475392AG39GENIChomozygous52062271