chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109789570109789571CT18GENIChomozygous884090079
10109792643109792644AG5GENICheterozygous884090080
10109792803109792804GA8GENIChomozygous884090081
10109792930109792931AT13GENIChomozygous884090082
10109793512109793513CA15GENIChomozygous884090083
10109793911109793912GA14GENIChomozygous884090084
10109794951109794952CA9GENIChomozygous884090085