chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	56374373	56374374	A	T	56	GENIC	homozygous	116500966
8	56374744	56374745	C	T	56	GENIC	homozygous	116500968
8	56375269	56375270	C	T	52	GENIC	homozygous	116500970
8	56376677	56376678	G	A	59	GENIC	homozygous	116500972
8	56377159	56377160	G	A	58	GENIC	homozygous	116500974
8	56377615	56377616	G	A	58	GENIC	homozygous	116500976
8	56378119	56378120	A	G	58	GENIC	homozygous	116500978
8	56378686	56378687	A		26	GENIC	homozygous	128593042
8	56378673	56378674	C		31	GENIC	homozygous	128593039
8	56377170	56377171	T		52	GENIC	homozygous	128593036
8	56378642	56378642		AT	31	GENIC	possibly homozygous	128593037
8	56378662	56378663	A		32	GENIC	homozygous	128593038
8	56378682	56378683	A		28	GENIC	homozygous	128593040
8	56378684	56378685	A		28	GENIC	homozygous	128593041
8	56378583	56378636	TGCTGCAATACATAATTAGCTACGATATAAGATCATGTCGATGCAGGGTCTAG		31	GENIC	heterozygous	129949173
8	56379629	56379659	CTCAGCCAGATTTTGTTAGTTCCCTTTGTG		1	GENIC	homozygous	131884706
8	56379663	56379668	ATCTG		1	GENIC	homozygous	131884707
8	56379670	56379681	CAGAAAAAAAC		1	GENIC	homozygous	131884708
8	56380262	56380263	T	G	45	GENIC	possibly homozygous	116500982
8	56380431	56380432	A	G	62	GENIC	homozygous	116500984
8	56381313	56381314	C	T	59	GENIC	homozygous	116500986
8	56381392	56381393	C	T	71	GENIC	homozygous	116500988
8	56382048	56382052	CAGA		69	GENIC	homozygous	128593044
8	56383021	56383022	C	A	66	GENIC	possibly homozygous	116500990
8	56383119	56383120	G	A	66	GENIC	homozygous	116500992
8	56383505	56383506	C	T	58	GENIC	homozygous	116500994
8	56384281	56384282	C	T	58	GENIC	homozygous	116500996
8	56384424	56384425	C	T	66	GENIC	homozygous	116500998
8	56384618	56384619	C	T	64	GENIC	homozygous	116501000
8	56386410	56386411	G	A	67	GENIC	homozygous	116501004
8	56389620	56389621	G	A	55	GENIC	homozygous	116501006
8	56390181	56390182	C	T	49	GENIC	homozygous	116501008
8	56390883	56390884	G	A	52	GENIC	homozygous	116501010
8	56392004	56392005	G	T	64	GENIC	homozygous	116501012
8	56393024	56393025	T	C	39	GENIC	homozygous	116501014