chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	76010636	76010637	A	G	26	GENIC	homozygous	110408388
18	76010706	76010707	G	A	25	GENIC	homozygous	110408390
18	76010772	76010773	C	T	25	GENIC	homozygous	110886481
18	76010781	76010782	T	C	23	GENIC	homozygous	110886483
18	76010788	76010789	C	T	23	GENIC	homozygous	110886485
18	76010793	76010794	C	T	22	GENIC	homozygous	110886487
18	76010797	76010798	A	G	21	GENIC	homozygous	110886489
18	76010823	76010824	T	C	26	GENIC	homozygous	119502116
18	76010824	76010825	G	A	26	GENIC	homozygous	119502117
18	76010839	76010840	G	T	30	GENIC	homozygous	119502118
18	76010900	76010901	C	T	30	GENIC	homozygous	119539793
18	76010901	76010902	A	G	30	GENIC	homozygous	119539794
18	76010904	76010905	G	A	30	GENIC	homozygous	119502119
18	76010944	76010945	A	C	33	GENIC	homozygous	119502120
18	76010946	76010947	T	C	33	GENIC	homozygous	119502121
18	76010975	76010976	C	G	35	GENIC	homozygous	119502122
18	76011016	76011017	A	G	46	GENIC	homozygous	119502123