chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	56203897	56203898	A	G	17	GENIC	homozygous	51654670
10	56204012	56204013	A	G	24	GENIC	homozygous	51654672
10	56204018	56204019	A	G	24	GENIC	homozygous	51654674
10	56204387	56204388	A	G	38	GENIC	homozygous	51654676
10	56204463	56204464	A	G	35	GENIC	homozygous	51654678
10	56206094	56206095	C	T	36	GENIC	homozygous	51891265
10	56206973	56206974	T	G	19	GENIC	homozygous	51654688
10	56207117	56207118	G	GC	13	GENIC	homozygous	51460011
10	56207127	56207133	TCTTAT	------	13	GENIC	homozygous	52377699
10	56207133	56207134	G	GAGA	12	GENIC	homozygous	52377702
10	56207135	56207136	G	C	12	GENIC	homozygous	51460014
10	56207177	56207178	C	CA	2	GENIC	heterozygous	52377704
10	56207801	56207803	TT	--	16	GENIC	homozygous	51654692
10	56208354	56208355	A	G	39	GENIC	homozygous	51654696
10	56208817	56208818	T	C	25	GENIC	homozygous	51654698
10	56209179	56209180	T	C	25	GENIC	homozygous	51654700
10	56209644	56209645	G	A	20	GENIC	homozygous	51891268
10	56209705	56209706	A	AGAAG	23	GENIC	homozygous	51654702
10	56209892	56209893	A	G	17	GENIC	homozygous	51654704
10	56211630	56211631	G	A	14	GENIC	homozygous	51891274