chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104108485104108486TTC35GENIChomozygous51589164
10104110474104110475CA5GENIChomozygous51589167
10104110597104110598A-12GENICheterozygous51589171
10104110621104110622GGGTT15GENICpossibly homozygous51589173
10104112870104112871CCT12GENIChomozygous51589175
10104112874104112875T-11GENIChomozygous51589177
10104114172104114173A-19GENIChomozygous51589179