chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	242107946	242107947	G	GT	17	GENIC	possibly homozygous	61136169
1	242107964	242107965	G	GA	18	GENIC	possibly homozygous	61136170
1	242108561	242108562	T	C	38	GENIC	homozygous	61136171
1	242109616	242109617	A	G	39	GENIC	homozygous	61136172
1	242109687	242109688	C	CTT	32	GENIC	heterozygous	62655713
1	242109688	242109689	T	-	32	GENIC	possibly homozygous	61623885
1	242111737	242111738	G	GCACA	11	GENIC	heterozygous	62250838
1	242112448	242112449	A	AC	21	GENIC	possibly homozygous	61136173
1	242112822	242112823	G	A	34	GENIC	homozygous	61136174
1	242113547	242113548	C	T	40	GENIC	homozygous	61136175
1	242114398	242114399	A	ATC	24	GENIC	homozygous	61136176
1	242114516	242114517	G	GT	19	GENIC	heterozygous	61136177
1	242114516	242114517	G	GTT	19	GENIC	heterozygous	62237797
1	242115682	242115683	C	A	30	GENIC	homozygous	61136178
1	242111737	242111738	G	GCACACACA	11	GENIC	possibly homozygous	62205946
1	242111893	242111894	G	GA	24	GENIC	heterozygous	62205948