chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22178758	22178759	A	C	46	GENIC	homozygous	115280579
12	22178869	22178870	C	T	47	GENIC	homozygous	115366487
12	22179603	22179604	C	A	35	GENIC	homozygous	115280581
12	22179607	22179608	G	A	34	GENIC	homozygous	115280583
12	22179618	22179619	T	C	35	GENIC	homozygous	115280585
12	22180896	22180897	T	C	16	GENIC	possibly homozygous	115280587
12	22182029	22182030	G	C	29	GENIC	homozygous	115280589
12	22182935	22182936	G	A	35	GENIC	homozygous	115280591
12	22182975	22182976	T	C	26	GENIC	homozygous	115280593
12	22185472	22185473	T	C	22	GENIC	homozygous	115280595
12	22186123	22186124	T	C	35	GENIC	homozygous	115280597
12	22187549	22187550	T	C	26	GENIC	homozygous	115280599
12	22187605	22187606	G	A	26	GENIC	homozygous	115280601
12	22188063	22188064	T	C	21	GENIC	homozygous	115280603
12	22188130	22188131	T	C	9	GENIC	homozygous	115280605
12	22189624	22189625	G	T	29	GENIC	homozygous	115280607
12	22190872	22190873	A	T	35	GENIC	possibly homozygous	115280609
12	22191051	22191052	T	A	20	GENIC	possibly homozygous	115280611
12	22191564	22191565	T	A	27	GENIC	homozygous	115280613
12	22191722	22191723	G	C	21	GENIC	homozygous	115280615
12	22192039	22192040	G	A	21	GENIC	homozygous	115280617
12	22192336	22192337	T	C	24	GENIC	homozygous	115280619
12	22192939	22192940	C	G	17	GENIC	possibly homozygous	115280621
12	22193015	22193016	C	T	14	GENIC	homozygous	115280623
12	22193182	22193183	T	C	18	GENIC	homozygous	115280625
12	22193919	22193920	G	A	33	GENIC	homozygous	115280627