chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2180187	2180188	G	T	34	GENIC	homozygous	115512592
12	2184049	2184050	A	G	26	GENIC	homozygous	115233787
12	2182350	2182351	A	G	27	GENIC	homozygous	115413881
12	2183491	2183492	G	A	27	GENIC	homozygous	115357274
12	2184005	2184006	G	A	21	GENIC	homozygous	115357276
12	2184157	2184158	G	C	30	GENIC	homozygous	115357277
12	2186804	2186805	T	C	27	GENIC	homozygous	115233791
12	2186884	2186885	T	G	24	GENIC	homozygous	115233793
12	2186938	2186939	G	A	26	GENIC	homozygous	115357279
12	2187018	2187019	A	G	29	GENIC	homozygous	115233795
12	2187306	2187307	A	G	20	GENIC	homozygous	115233797
12	2187582	2187583	C	T	23	GENIC	homozygous	115233799
12	2188003	2188004	A	C	25	GENIC	homozygous	115512593
12	2188430	2188431	A	G	31	GENIC	homozygous	115233803
12	2188826	2188827	C	G	26	GENIC	homozygous	115233805
12	2191340	2191341	G	C	24	GENIC	homozygous	115233817
12	2191402	2191403	T	C	19	GENIC	homozygous	115233819
12	2191452	2191453	T	A	11	GENIC	homozygous	115233821
12	2191720	2191721	C	G	14	GENIC	homozygous	115233825
12	2191799	2191800	G	A	14	GENIC	homozygous	115357285