chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	43250877	43250878	C	CT	7	GENIC	possibly homozygous	52371934
10	43250880	43250881	T	-	7	GENIC	heterozygous	52722379
10	43253171	43253177	TTTTTT	------	6	GENIC	heterozygous	52371936
10	43253172	43253177	TTTTT	-----	6	GENIC	heterozygous	52371938
10	43250977	43250981	CTTA	----	17	GENIC	homozygous	52147500
10	43252340	43252341	T	C	13	GENIC	homozygous	52147502
10	43251051	43251054	TTC	---	16	GENIC	homozygous	52190870
10	43252139	43252140	A	AAGG	13	GENIC	homozygous	52190872
10	43252262	43252263	T	C	16	GENIC	homozygous	52190874
10	43251054	43251055	G	A	16	GENIC	homozygous	52317294
10	43252690	43252691	C	-	31	GENIC	homozygous	51435069