chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11241490	11241491	G	C	61	GENIC	possibly homozygous	115580392
12	11241923	11241924	C	G	67	GENIC	homozygous	115580394
12	11243893	11243894	T	G	49	GENIC	homozygous	115254912
12	11244780	11244781	A	G	65	GENIC	homozygous	115254914
12	11244834	11244835	G	A	60	GENIC	homozygous	115361397
12	11246821	11246822	G	A	60	GENIC	possibly homozygous	115254916
12	11247876	11247877	C	T	43	GENIC	homozygous	115580396
12	11249703	11249704	A	G	41	GENIC	possibly homozygous	118244405
12	11249828	11249829	G	A	37	GENIC	homozygous	115254918
12	11247763	11247764	T	C	20	GENIC	heterozygous	118291906
12	11247767	11247768	A	G	22	GENIC	homozygous	118291907
12	11249377	11249378	C	T	42	GENIC	homozygous	118291908