chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46760719767607198CT44INTERGENIChomozygous774990854
46760735667607357CT33GENIChomozygous774990855
46760793867607939AG39GENIChomozygous774990856
46760795167607952AT41GENIChomozygous774990857
46760828267608283GC45GENIChomozygous774990858
46760894767608948CA18GENICheterozygous774990859
46760907467609075TG51GENIChomozygous774990860
46760915467609155AC35GENIChomozygous774990861
46761015867610159GA41GENIChomozygous774990862
46761017167610172AG36GENIChomozygous774990863
46761189467611895AT37GENIChomozygous774990864
46761212467612125TA35GENIChomozygous774990865
46761392767613928AC31GENIChomozygous774990866
46761474867614749CT29GENIChomozygous774990867
46761505367615054GA34GENIChomozygous774990868
46761507967615080AT36GENIChomozygous774990869
46761509067615091TC33GENIChomozygous774990870
46761592667615927AT46GENICpossibly homozygous774990871