chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59123147	59123148	C	T	11	GENIC	homozygous	116511053
8	59123153	59123154	C	A	11	GENIC	homozygous	116511055
8	59123188	59123189	T	C	12	GENIC	homozygous	116511057
8	59123193	59123194	T	C	12	GENIC	homozygous	116511059
8	59123521	59123522	A	G	13	GENIC	homozygous	116511061
8	59123570	59123571	T		10	GENIC	homozygous	128595528
8	59123871	59123872	T	C	25	GENIC	homozygous	116511063
8	59124563	59124564	T	C	20	GENIC	homozygous	116511065
8	59124615	59124616	G	A	20	GENIC	homozygous	116511067
8	59124910	59124911	T	C	9	GENIC	homozygous	117157633
8	59124912	59124913	C	G	9	GENIC	homozygous	117157634
8	59124920	59124921	G	T	9	GENIC	homozygous	117157635
8	59125238	59125239	A	G	29	GENIC	homozygous	116511069
8	59129271	59129272	C	T	21	GENIC	homozygous	116511071
8	59132175	59132176	G	A	10	GENIC	homozygous	116511087
8	59133387	59133388	A	G	20	GENIC	homozygous	116511089
8	59133665	59133666	T	C	23	GENIC	homozygous	116511091
8	59134060	59134061	C	T	15	GENIC	homozygous	116511093
8	59134417	59134418	G	A	24	GENIC	homozygous	116511095
8	59136009	59136010	G	T	23	GENIC	homozygous	116511115
8	59136066	59136067	G	A	21	GENIC	homozygous	116511117
8	59136902	59136903	G	A	18	GENIC	homozygous	116511119
8	59138199	59138200	C	G	15	GENIC	homozygous	116511121
8	59139625	59139626	C	A	22	GENIC	homozygous	116511123