chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11204007	11204008	G	A	21	GENIC	possibly homozygous	115594747
12	11206342	11206343	A	C	22	GENIC	possibly homozygous	115594749
12	11208303	11208304	C	T	18	GENIC	possibly homozygous	115594751
12	11208717	11208718	T	C	18	GENIC	homozygous	115254818
12	11208742	11208743	T	C	13	GENIC	homozygous	115254820
12	11208945	11208946	C	T	26	GENIC	homozygous	115594753
12	11209532	11209533	T	C	29	GENIC	homozygous	115254824
12	11209548	11209549	G	A	33	GENIC	homozygous	115594755
12	11209657	11209658	T	C	27	GENIC	homozygous	115254826
12	11211493	11211494	G	T	20	GENIC	homozygous	115254834
12	11211530	11211531	T	C	15	GENIC	possibly homozygous	115361393
12	11212326	11212327	A	G	23	GENIC	homozygous	115254844
12	11212410	11212411	C	T	24	GENIC	homozygous	115254846
12	11213411	11213412	G	A	25	GENIC	possibly homozygous	115254852