chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46760719767607198CT40GENIChomozygous928850537
46760735667607357CT31GENIChomozygous928850538
46760793867607939AG36GENIChomozygous928850539
46760795167607952AT37GENIChomozygous928850540
46760828267608283GC40GENIChomozygous928850541
46760894767608948CA15GENIChomozygous928850542
46760907467609075TG44GENIChomozygous928850543
46760915467609155AC34GENIChomozygous928850544
46761015867610159GA34GENIChomozygous928850545
46761017167610172AG31GENIChomozygous928850546
46761189467611895AT30GENIChomozygous928850547
46761212467612125TA30GENIChomozygous928850548
46761505367615054GA34GENIChomozygous928850549
46761507967615080AT35GENIChomozygous928850550
46761509067615091TC31GENIChomozygous928850551
46761592667615927AT36GENICpossibly homozygous928850552