chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	6696762	6696763	C	T	35	GENIC	homozygous	115235228
6	6696891	6696892	T	C	28	GENIC	homozygous	115235230
6	6697907	6697908	C	A	36	GENIC	homozygous	115235232
6	6698101	6698102	G	C	28	GENIC	homozygous	114715489
6	6698394	6698395	C	T	29	GENIC	homozygous	115235234
6	6698778	6698779	C	A	52	GENIC	homozygous	115040465
6	6699011	6699012	C	T	30	GENIC	homozygous	115235236
6	6700190	6700191	T	C	27	GENIC	homozygous	115235238
6	6700561	6700562	G	A	30	GENIC	possibly homozygous	115235240
6	6700851	6700852	T	C	43	GENIC	homozygous	115040466
6	6701752	6701753	T	G	26	GENIC	possibly homozygous	115235242
6	6702069	6702070	G	C	40	GENIC	homozygous	115040467
6	6702076	6702077	A	C	36	GENIC	homozygous	115235244
6	6702354	6702355	G	A	33	GENIC	possibly homozygous	115235246
6	6703086	6703087	C	T	20	GENIC	homozygous	115235248
6	6705627	6705628	C	T	19	GENIC	possibly homozygous	115235250
6	6707584	6707585	G	A	23	GENIC	homozygous	115235252
6	6707700	6707701	G	A	28	GENIC	homozygous	115235254
6	6709054	6709055	G	A	19	GENIC	homozygous	115235256
6	6709533	6709534	T	A	27	GENIC	homozygous	115040472
6	6709748	6709749	T	C	43	GENIC	homozygous	115235258
6	6704813	6704814	T	C	16	GENIC	heterozygous	115367740
6	6704844	6704845	C	T	8	GENIC	heterozygous	115367742