chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	113200475	113200476	G	A	45	GENIC	homozygous	138660371
9	113205279	113205279		T	45	GENIC	possibly homozygous	138481215
9	113220317	113220318	C	T	47	GENIC	homozygous	138660372
9	113221933	113221934	T	C	33	GENIC	homozygous	138660373
9	113222412	113222413	G	A	43	GENIC	homozygous	138660374
9	113226503	113226504	A	G	41	GENIC	homozygous	138660375
9	113231606	113231607	A	G	58	GENIC	homozygous	138660376
9	113232003	113232004	G	A	48	GENIC	homozygous	138660377
9	113233630	113233630		T	46	GENIC	possibly homozygous	138481216
9	113235498	113235499	G	T	52	GENIC	possibly homozygous	138660378
9	113237750	113237750		T	46	GENIC	possibly homozygous	138481217
9	113245294	113245295	G	A	43	GENIC	homozygous	138660379
9	113246870	113246871	G	T	30	GENIC	homozygous	138660380
9	113248043	113248044	T	G	33	GENIC	homozygous	138660381
9	113254852	113254853	C	T	38	GENIC	homozygous	138660382
9	113263077	113263078	A		41	GENIC	homozygous	138481218
9	113263799	113263799		ATACTGGACAAAA	48	GENIC	homozygous	138481219
9	113265326	113265327	A	G	41	GENIC	homozygous	138660383
9	113275544	113275545	A		31	GENIC	heterozygous	138481220