chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	206287760	206287761	A	G	30	GENIC	homozygous	74683100
1	206288948	206288949	G	A	33	GENIC	homozygous	74683102
1	206289842	206289843	A	G	27	GENIC	homozygous	74683106
1	206289843	206289844	T	A	28	GENIC	homozygous	75206375
1	206295194	206295195	G	A	30	GENIC	possibly homozygous	74683126
1	206309801	206309802	G	A	38	GENIC	homozygous	74683128
1	206311309	206311310	A	G	20	GENIC	homozygous	74683130
1	206313063	206313064	C	G	19	GENIC	heterozygous	75735778
1	206313757	206313758	G	A	35	GENIC	homozygous	74683132
1	206314877	206314878	G	A	30	GENIC	homozygous	74683134
1	206317750	206317751	T	C	25	GENIC	homozygous	74683136
1	206317832	206317833	T	C	14	GENIC	homozygous	74683138
1	206318531	206318532	G	A	26	GENIC	possibly homozygous	74683140
1	206319282	206319283	C	A	8	GENIC	homozygous	74683142
1	206323084	206323085	A	G	33	GENIC	possibly homozygous	74683144
1	206323340	206323341	A	C	30	GENIC	homozygous	74683146
1	206324839	206324840	G	C	19	GENIC	homozygous	74683148
1	206328300	206328301	G	A	24	GENIC	homozygous	74683150
1	206329506	206329507	A	C	21	GENIC	homozygous	74683152
1	206329809	206329810	A	T	31	GENIC	possibly homozygous	74683154
1	206332270	206332271	A	G	30	GENIC	homozygous	74683156
1	206332467	206332468	A	G	33	GENIC	homozygous	74683158
1	206334379	206334380	T	G	42	GENIC	homozygous	74683162
1	206336771	206336772	G	A	23	GENIC	homozygous	74683164
1	206337122	206337123	C	T	43	GENIC	homozygous	74683166
1	206337401	206337402	A	G	21	GENIC	homozygous	74683168
1	206341583	206341584	C	T	30	GENIC	possibly homozygous	74683170