chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105946678359466784T-18GENIChomozygous51897669
105946797359468001AGAGAGAGAGAGAGAGAGAGAGAGAGAG----------------------------4GENIChomozygous52379090
105947223259472233CG20GENIChomozygous51465616
105947225459472255GA25GENIChomozygous51897689
105947229959472300CT22GENIChomozygous51897691
105947261459472624CCAAACCAAA----------4GENIChomozygous52460861
105947323759473238TC35GENICpossibly homozygous52062259
105946825859468259GA28GENIChomozygous52062253
105947281759472818TC28GENIChomozygous52062255
105947296259472963AG33GENIChomozygous52062257
105947413659474137TA29GENIChomozygous52062261
105947452359474524GA37GENIChomozygous52062263
105947471759474718AG22GENIChomozygous52062265
105947475359474754GA22GENIChomozygous52062267
105947512459475125AC34GENIChomozygous52062269
105947539159475392AG20GENIChomozygous52062271