chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	90971467	90971468	C	T	18	GENIC	homozygous	51035717
11	90973210	90973211	T	-	14	GENIC	homozygous	50864760
11	90978686	90978687	G	T	19	GENIC	homozygous	51035718
11	90978710	90978711	G	C	16	GENIC	homozygous	51035719
11	90979118	90979119	A	AAC	17	GENIC	homozygous	50864765
11	90979174	90979175	T	C	11	GENIC	homozygous	51035720
11	90979534	90979535	C	CTTT	11	GENIC	heterozygous	50975151
11	90979534	90979535	C	CTT	11	GENIC	possibly homozygous	50975152
11	90979703	90979704	T	C	12	GENIC	homozygous	51035721
11	90979974	90979975	T	TTGTGTG	18	GENIC	homozygous	50975155
11	90980139	90980140	G	T	19	GENIC	homozygous	51035722