chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2182350	2182351	A	G	47	GENIC	homozygous	115413881
12	2182447	2182448	C	T	46	GENIC	homozygous	115357273
12	2183491	2183492	G	A	45	GENIC	homozygous	115357274
12	2183648	2183649	T	C	42	GENIC	homozygous	115357275
12	2184005	2184006	G	A	17	GENIC	homozygous	115357276
12	2184049	2184050	A	G	20	GENIC	homozygous	115233787
12	2184157	2184158	G	C	31	GENIC	homozygous	115357277
12	2184507	2184508	G	A	41	GENIC	homozygous	115357278
12	2186804	2186805	T	C	19	GENIC	homozygous	115233791
12	2186884	2186885	T	G	25	GENIC	homozygous	115233793
12	2186938	2186939	G	A	32	GENIC	homozygous	115357279
12	2187018	2187019	A	G	35	GENIC	homozygous	115233795
12	2187306	2187307	A	G	45	GENIC	homozygous	115233797
12	2187582	2187583	C	T	22	GENIC	homozygous	115233799
12	2187724	2187725	G	A	17	GENIC	homozygous	115357280
12	2188430	2188431	A	G	31	GENIC	homozygous	115233803
12	2188758	2188759	G	A	32	GENIC	homozygous	115357281
12	2188826	2188827	C	G	27	GENIC	homozygous	115233805
12	2190187	2190188	G	A	24	GENIC	homozygous	115357282
12	2190540	2190541	G	A	37	GENIC	homozygous	115357283
12	2191266	2191267	T	G	27	GENIC	homozygous	115357284
12	2191340	2191341	G	C	28	GENIC	homozygous	115233817
12	2191402	2191403	T	C	34	GENIC	homozygous	115233819
12	2191452	2191453	T	A	31	GENIC	homozygous	115233821
12	2191720	2191721	C	G	26	GENIC	homozygous	115233825
12	2191799	2191800	G	A	25	GENIC	homozygous	115357285