chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	205862652	205862653	C	G	26	GENIC	homozygous	135793638
1	205863721	205863722	G	A	14	GENIC	possibly homozygous	135793639
1	205864081	205864082	C	T	19	GENIC	homozygous	135793640
1	205864150	205864151	A	G	22	GENIC	homozygous	135793641
1	205864206	205864207	A	C	24	GENIC	homozygous	135793642
1	205864238	205864239	A	G	27	GENIC	homozygous	135793643
1	205864928	205864929	G	A	13	GENIC	homozygous	135793644
1	205865269	205865270	T	A	22	GENIC	homozygous	135793645
1	205866201	205866202	G	T	22	GENIC	homozygous	135793646
1	205866217	205866218	G	A	18	GENIC	homozygous	135793647
1	205869085	205869086	C	A	16	GENIC	homozygous	135793648
1	205869242	205869242		AA	16	GENIC	homozygous	135456180
1	205864634	205864635	T		26	GENIC	homozygous	135456177
1	205867765	205867765		T	17	GENIC	homozygous	135456178
1	205868712	205868712		TTA	16	GENIC	homozygous	135456179
1	205869615	205869616	G	A	25	GENIC	homozygous	135793649
1	205869661	205869661		TGTGCT	20	GENIC	homozygous	135456181
1	205870382	205870383	C	T	22	GENIC	homozygous	135793650
1	205870383	205870384	C	G	23	GENIC	homozygous	135793651