chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	26089346	26089347	T	TTGCTC	14	GENIC	homozygous	50145578
12	26089356	26089357	C	A	15	GENIC	homozygous	50145580
12	26089650	26089651	A	G	11	GENIC	homozygous	50145582
12	26090022	26090023	G	A	27	GENIC	homozygous	50145584
12	26090042	26090043	G	A	23	GENIC	homozygous	50145586
12	26090202	26090203	C	G	26	GENIC	homozygous	50145588
12	26090563	26090564	A	C	21	GENIC	homozygous	50145590
12	26090852	26090853	T	TGTGTGTGTGTGTGTGTGTGTGTGTG	7	GENIC	possibly homozygous	50614622
12	26095149	26095150	G	GAA	19	GENIC	heterozygous	50145593
12	26095149	26095150	G	GA	19	GENIC	heterozygous	50145595
12	26096013	26096014	C	T	18	GENIC	homozygous	50145597
12	26097587	26097595	GTGTGTGT	--------	9	GENIC	homozygous	50145601