chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41639041	41639042	T	A	34	GENIC	homozygous	115330976
12	41639321	41639322	A	T	37	GENIC	homozygous	115330978
12	41639322	41639323	T	A	37	GENIC	homozygous	115330980
12	41639604	41639605	A	C	29	GENIC	homozygous	115330982
12	41639605	41639606	C	A	29	GENIC	homozygous	115330984
12	41639833	41639834	C	T	41	GENIC	homozygous	115330986
12	41639834	41639835	T	C	41	GENIC	homozygous	115330988
12	41643140	41643141	G	A	21	GENIC	homozygous	115427012
12	41643842	41643843	A	C	22	GENIC	homozygous	115330992
12	41646090	41646091	G	C	51	GENIC	homozygous	115385556
12	41646188	41646189	T	C	30	GENIC	homozygous	115330998
12	41646341	41646342	C	T	45	GENIC	homozygous	115427014