chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16016426	16016427	T	C	18	GENIC	homozygous	50076243
12	16017201	16017207	TGTGTG	------	21	GENIC	homozygous	50502604
12	16020255	16020256	T	C	31	GENIC	homozygous	50076250
12	16020974	16020975	A	T	32	GENIC	homozygous	50076256
12	16021182	16021183	G	A	33	GENIC	homozygous	50076258
12	16021286	16021287	T	G	35	GENIC	homozygous	50076260
12	16022336	16022337	A	C	38	GENIC	homozygous	50076262
12	16022790	16022791	G	A	31	GENIC	homozygous	50504110
12	16024976	16024977	C	T	29	GENIC	homozygous	50504111
12	16026015	16026016	T	C	29	INTERGENIC	homozygous	50076294
12	16026909	16026917	TTTTTTTT	--------	14	INTERGENIC	heterozygous	50534203
12	16027447	16027448	G	A	33	INTERGENIC	homozygous	50504112
12	16028369	16028370	C	T	19	INTERGENIC	homozygous	50076300
12	16028410	16028411	G	GT	23	INTERGENIC	homozygous	50502615
12	16028353	16028354	C	CA	16	INTERGENIC	homozygous	50568839