chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103606854103606855AG21GENIChomozygous52078546
10103607003103607004CT22GENIChomozygous52078548
10103607078103607079GT29GENICpossibly homozygous52078550
10103607113103607114GA25GENIChomozygous52078552
10103607394103607395CT34GENIChomozygous52328233
10103607763103607764CT23GENIChomozygous52328235
10103608027103608028AC31GENIChomozygous52078554
10103608567103608568AG30GENIChomozygous52078558
10103609344103609345AG29GENIChomozygous52078564
10103609353103609354CT28GENIChomozygous52078566
10103609392103609393GC31GENIChomozygous53175436