chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103186905	103186906	C	T	13	GENIC	homozygous	61487785
1	103187133	103187134	T	C	38	GENIC	homozygous	61487786
1	103187210	103187211	G	C	36	GENIC	homozygous	61487787
1	103187234	103187235	T	TG	13	GENIC	heterozygous	60780208
1	103187234	103187235	T	TGG	13	GENIC	heterozygous	61487788
1	103187479	103187480	A	G	33	GENIC	homozygous	61487789
1	103187761	103187762	C	T	26	GENIC	homozygous	61487790
1	103187835	103187836	G	A	21	GENIC	homozygous	61487791
1	103188019	103188020	C	T	30	GENIC	homozygous	61487792
1	103188214	103188215	G	C	25	GENIC	homozygous	61487794
1	103188907	103188908	A	G	43	GENIC	homozygous	61487795
1	103188928	103188929	A	G	38	GENIC	homozygous	61487796
1	103189084	103189085	C	T	35	GENIC	homozygous	61487797
1	103189941	103189942	C	T	27	GENIC	homozygous	61487798