chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71518093915180940GA41GENIChomozygous116115434
71518171715181718TC50GENIChomozygous115576522
71518299815182999TG39GENICpossibly homozygous116115435
71518721915187220TC34GENIChomozygous116004589
71518735415187355CT37GENIChomozygous116115437
71518751315187514TC40GENIChomozygous116004590
71518752015187521CT42GENIChomozygous116004591
71518797415187975TC36GENIChomozygous116004593
71518823915188240GA47GENICheterozygous116004594
71518830915188310CT31GENIChomozygous116004595
71518914715189148TC49GENIChomozygous116004596
71518948615189487AG40GENIChomozygous116004597
71518965015189651AC34GENIChomozygous116004598
71519018415190185CG39GENIChomozygous116004599
71519051815190519AG40GENIChomozygous116004600