chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	87435113	87435114	C	G	1	GENIC	homozygous	51030158
11	87435335	87435336	A	G	3	GENIC	homozygous	51171061
11	87435657	87435658	C	T	2	GENIC	heterozygous	51030171
11	87435660	87435661	T	C	3	GENIC	heterozygous	51030172
11	87435683	87435684	C	G	10	GENIC	homozygous	51030173
11	87435879	87435880	C	G	25	GENIC	possibly homozygous	51030174
11	87436010	87436011	C	T	12	GENIC	homozygous	51030175
11	87436055	87436056	T	C	12	GENIC	homozygous	51030176
11	87436603	87436604	G	A	29	GENIC	heterozygous	51030177
11	87437516	87437517	T	C	11	GENIC	homozygous	51030178
11	87438240	87438241	C	T	21	GENIC	homozygous	51030181
11	87438546	87438547	G	A	19	GENIC	possibly homozygous	51030182
11	87441137	87441138	G	A	18	GENIC	homozygous	51030186
11	87442043	87442044	C	G	27	GENIC	homozygous	51030187
11	87442235	87442236	G	A	13	GENIC	heterozygous	51030188
11	87442403	87442404	A	-	7	GENIC	homozygous	51030189
11	87442714	87442719	TAATC	-----	7	GENIC	homozygous	51030190
11	87442927	87442928	G	GTA	2	GENIC	heterozygous	51171063
11	87442936	87442942	TGTGTT	------	2	GENIC	heterozygous	51030191
11	87442961	87442962	G	GTGTT	2	GENIC	homozygous	51171064
11	87443039	87443065	TGTGTGTGTGTGTGTGCGTGCGTGCA	--------------------------	2	GENIC	homozygous	51030193
11	87443219	87443220	T	C	17	GENIC	possibly homozygous	51030194
11	87443220	87443221	T	C	17	GENIC	possibly homozygous	51030195
11	87444371	87444372	T	C	17	GENIC	possibly homozygous	51030196