chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2183474	2183475	G	A	40	GENIC	homozygous	115233783
12	2184048	2184049	C	T	33	GENIC	homozygous	115233785
12	2184049	2184050	A	G	33	GENIC	homozygous	115233787
12	2186123	2186124	T	C	59	GENIC	homozygous	115233789
12	2186804	2186805	T	C	53	GENIC	homozygous	115233791
12	2186884	2186885	T	G	58	GENIC	homozygous	115233793
12	2187018	2187019	A	G	48	GENIC	homozygous	115233795
12	2187306	2187307	A	G	51	GENIC	homozygous	115233797
12	2187582	2187583	C	T	46	GENIC	homozygous	115233799
12	2187773	2187774	C	T	42	GENIC	homozygous	115233801
12	2188430	2188431	A	G	45	GENIC	homozygous	115233803
12	2188826	2188827	C	G	40	GENIC	homozygous	115233805
12	2189129	2189130	G	A	60	GENIC	homozygous	115233807
12	2189446	2189447	C	T	37	GENIC	homozygous	115233809
12	2189452	2189453	A	T	37	GENIC	homozygous	115233811
12	2190018	2190019	G	A	39	GENIC	possibly homozygous	115233813
12	2190426	2190427	G	A	50	GENIC	homozygous	115233815
12	2191340	2191341	G	C	53	GENIC	possibly homozygous	115233817
12	2191402	2191403	T	C	60	GENIC	homozygous	115233819
12	2191452	2191453	T	A	49	GENIC	homozygous	115233821
12	2191538	2191539	C	T	43	GENIC	homozygous	115233823
12	2191720	2191721	C	G	43	GENIC	homozygous	115233825
12	2191762	2191763	G	A	42	GENIC	homozygous	115233827
12	2191789	2191790	C	T	46	GENIC	homozygous	115233829