chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	56376677	56376678	G	A	60	GENIC	homozygous	116500972
8	56377170	56377171	T		63	GENIC	homozygous	128593036
8	56377615	56377616	G	A	46	GENIC	homozygous	116500976
8	56378119	56378120	A	G	49	GENIC	homozygous	116500978
8	56378583	56378636	TGCTGCAATACATAATTAGCTACGATATAAGATCATGTCGATGCAGGGTCTAG		28	GENIC	heterozygous	129949173
8	56378642	56378642		AT	28	GENIC	possibly homozygous	128593037
8	56378662	56378663	A		26	GENIC	homozygous	128593038
8	56378673	56378674	C		24	GENIC	homozygous	128593039
8	56378682	56378683	A		24	GENIC	homozygous	128593040
8	56378684	56378685	A		24	GENIC	homozygous	128593041
8	56378686	56378687	A		23	GENIC	homozygous	128593042
8	56380262	56380263	T	G	38	GENIC	homozygous	116500982
8	56380431	56380432	A	G	40	GENIC	homozygous	116500984
8	56381313	56381314	C	T	54	GENIC	homozygous	116500986
8	56381392	56381393	C	T	51	GENIC	homozygous	116500988
8	56382048	56382052	CAGA		53	GENIC	homozygous	128593044
8	56382085	56382086	C	T	53	GENIC	homozygous	117942310
8	56383021	56383022	C	A	62	GENIC	homozygous	116500990
8	56383119	56383120	G	A	66	GENIC	homozygous	116500992
8	56383812	56383813	G	A	50	GENIC	homozygous	117942311
8	56386127	56386128	A		69	GENIC	homozygous	133189359
8	56387808	56387809	G	A	59	GENIC	homozygous	117942312
8	56389620	56389621	G	A	58	GENIC	possibly homozygous	116501006
8	56390458	56390459	G	A	48	GENIC	homozygous	117942313
8	56390809	56390810	A	G	52	GENIC	homozygous	118098755
8	56392004	56392005	G	T	58	GENIC	homozygous	116501012
8	56393024	56393025	T	C	47	GENIC	homozygous	116501014