chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	26402559	26402560	G	C	41	GENIC	homozygous	51371746
10	26402611	26402612	C	T	33	GENIC	homozygous	51371748
10	26402921	26402922	A	AT	8	GENIC	homozygous	51371750
10	26403093	26403094	T	G	22	GENIC	homozygous	51371752
10	26403132	26403133	T	C	21	GENIC	homozygous	51371754
10	26403171	26403172	T	TCAGCTACTGCTCATTG	25	GENIC	homozygous	51371756
10	26403795	26403796	G	A	11	GENIC	heterozygous	51371760
10	26403855	26403859	ACTT	----	12	GENIC	heterozygous	51371762
10	26404892	26404893	G	A	18	GENIC	homozygous	51371763
10	26404955	26404956	C	A	18	GENIC	homozygous	51371765
10	26405976	26405977	A	C	9	GENIC	homozygous	51371767
10	26407422	26407423	A	G	7	GENIC	homozygous	51371769
10	26408062	26408063	A	G	16	GENIC	homozygous	51371771
10	26409209	26409210	T	C	23	GENIC	homozygous	51371773
10	26415047	26415048	C	A	23	GENIC	homozygous	51371779
10	26415649	26415650	A	ACAAGCT	2	GENIC	homozygous	51371781
10	26415770	26415771	C	G	21	GENIC	possibly homozygous	51371783
10	26415800	26415801	T	C	23	GENIC	heterozygous	51371785
10	26415809	26415811	TC	--	20	GENIC	heterozygous	51371787
10	26415814	26415815	T	C	22	GENIC	heterozygous	51371789
10	26416089	26416090	A	ATCTTT	25	GENIC	homozygous	51371791
10	26416473	26416474	C	T	14	GENIC	homozygous	51371793
10	26416611	26416612	T	C	24	GENIC	homozygous	51371795
10	26417980	26417981	G	A	27	GENIC	homozygous	51371797
10	26418179	26418180	A	G	21	GENIC	homozygous	51371799
10	26418475	26418476	G	C	19	GENIC	homozygous	51371801
10	26418598	26418604	AGTAAA	------	5	GENIC	homozygous	51371803
10	26419343	26419376	CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA	---------------------------------	10	GENIC	homozygous	51371805
10	26410951	26410953	CA	--	9	GENIC	heterozygous	51633140