chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	56340976	56340977	T	A	26	GENIC	homozygous	52059151
10	56341634	56341635	A	AG	20	GENIC	possibly homozygous	52502530
10	56341918	56341919	A	AT	31	GENIC	homozygous	52059153
10	56342136	56342138	TT	--	10	GENIC	heterozygous	51986752
10	56342137	56342138	T	-	10	GENIC	heterozygous	51891816
10	56342179	56342180	T	TTG	3	GENIC	homozygous	52377761
10	56342184	56342185	T	TGCTAGGCAAGCGC	2	GENIC	homozygous	52377763
10	56342188	56342189	G	-	2	GENIC	homozygous	52377765
10	56343005	56343006	G	-	18	GENIC	homozygous	52059155
10	56347784	56347785	G	C	28	GENIC	possibly homozygous	51654988
10	56349997	56350000	TGG	---	16	INTERGENIC	homozygous	52059157
10	56351317	56351318	G	GC	3	GENIC	homozygous	51460063
10	56353307	56353308	A	G	26	GENIC	homozygous	52059159
10	56357138	56357151	AGTGATGCGATCT	-------------	29	GENIC	homozygous	52059161
10	56358993	56358994	C	CTGTG	1	GENIC	homozygous	52439803
10	56359147	56359149	TC	--	19	GENIC	homozygous	52059163
10	56363188	56363189	G	A	22	GENIC	homozygous	52059165
10	56363391	56363392	T	C	26	GENIC	homozygous	51654994
10	56364531	56364532	G	A	27	GENIC	possibly homozygous	51654996