chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52553860	52553861	A	G	50	GENIC	homozygous	114550519
13	52553914	52553915	C	A	48	GENIC	homozygous	114764940
13	52554489	52554490	G	T	47	GENIC	homozygous	115182545
13	52554979	52554980	T	A	18	GENIC	homozygous	131925119
13	52554981	52554982	T	A	18	GENIC	homozygous	131925120
13	52554983	52554984	T	A	19	GENIC	homozygous	131925121
13	52554985	52554986	T	A	19	GENIC	homozygous	131925122
13	52556265	52556266	A	G	54	GENIC	homozygous	114550521
13	52556353	52556354	G	A	66	GENIC	homozygous	114948944
13	52556838	52556841	CCT		55	GENIC	possibly homozygous	133261375
13	52556870	52556871	C		52	GENIC	homozygous	133261376
13	52556925	52556926	G	A	59	GENIC	homozygous	114550522
13	52557036	52557037	A	G	57	GENIC	homozygous	114764942
13	52557115	52557116	T	C	56	GENIC	homozygous	114764944
13	52559259	52559260	A	G	56	GENIC	homozygous	114550523
13	52559357	52559358	T	C	49	GENIC	homozygous	114550524
13	52561540	52561541	C	T	47	GENIC	homozygous	114550532
13	52562609	52562610	G	T	76	GENIC	homozygous	114550536
13	52557415	52557421	CTCTGG		70	GENIC	homozygous	131126802
13	52564174	52564175	C		30	GENIC	homozygous	133261377
13	52567709	52567710	T	C	56	GENIC	homozygous	114764946
13	52568195	52568196	C	T	63	GENIC	homozygous	114550543
13	52571481	52571481		ACATCTCT	57	GENIC	homozygous	131126807
13	52571482	52571483	G	T	54	GENIC	homozygous	114550546
13	52564166	52564167	T	C	38	GENIC	heterozygous	133267822
13	52564172	52564173	T	C	34	GENIC	possibly homozygous	133267823
13	52570664	52570665	T	C	51	GENIC	homozygous	114550545
13	52574579	52574580	T	C	57	GENIC	homozygous	114550549