chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	56377133	56377134	C	T	35	GENIC	possibly homozygous	117042164
8	56377443	56377444	A	C	41	GENIC	possibly homozygous	117042165
8	56378033	56378034	T	C	44	GENIC	homozygous	117042166
8	56378119	56378120	A	G	40	GENIC	homozygous	116500978
8	56379175	56379176	A	G	20	GENIC	homozygous	116500980
8	56380556	56380557	A	C	35	GENIC	homozygous	117042167
8	56382367	56382368	G	A	31	GENIC	homozygous	117042168
8	56383119	56383120	G	A	28	GENIC	homozygous	116500992
8	56386437	56386438	C	T	49	GENIC	possibly homozygous	117042169
8	56386547	56386548	G	C	29	GENIC	homozygous	117042170
8	56386608	56386609	G	A	35	GENIC	homozygous	117042171
8	56388276	56388277	C	T	35	GENIC	homozygous	117042172
8	56388793	56388794	C	A	34	GENIC	possibly homozygous	117042173
8	56389241	56389242	A	G	35	GENIC	homozygous	117042174
8	56389620	56389621	G	A	46	GENIC	possibly homozygous	116501006
8	56389696	56389697	G	A	39	GENIC	homozygous	117042175
8	56390624	56390625	C	G	20	GENIC	homozygous	117042176
8	56392004	56392005	G	T	52	GENIC	homozygous	116501012
8	56393024	56393025	T	C	20	GENIC	homozygous	116501014