chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12440783	12440784	T	C	48	GENIC	homozygous	115569960
7	12444390	12444391	A	C	29	GENIC	homozygous	115569961
7	12444432	12444433	C	T	28	GENIC	homozygous	115569962
7	12448795	12448796	C	A	41	GENIC	homozygous	115569963
7	12448894	12448895	G	A	44	GENIC	homozygous	115569964
7	12449579	12449580	G	A	20	GENIC	homozygous	115569966
7	12452278	12452279	A	G	36	GENIC	homozygous	115569970
7	12452554	12452555	A	G	50	GENIC	homozygous	115569971
7	12454665	12454666	C	T	31	GENIC	homozygous	115569974
7	12455144	12455145	C	T	42	GENIC	homozygous	115569975
7	12455157	12455158	G	C	42	GENIC	homozygous	115569976
7	12455254	12455255	C	G	28	GENIC	homozygous	115569977
7	12455306	12455307	C	T	20	GENIC	homozygous	115569978
7	12455817	12455818	C	A	26	GENIC	homozygous	115569986
7	12455825	12455826	G	A	27	GENIC	homozygous	115569987
7	12456134	12456135	A	C	31	GENIC	homozygous	115569988
7	12456168	12456169	C	T	33	GENIC	homozygous	115569989
7	12457365	12457366	T	C	19	GENIC	possibly homozygous	115569990