chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11033137	11033138	T	C	33	GENIC	homozygous	154425236
7	11033178	11033179	A	G	30	GENIC	homozygous	138004095
7	11034398	11034399	G	C	52	GENIC	homozygous	138004096
7	11034487	11034488	T	G	47	GENIC	homozygous	138004097
7	11035223	11035224	C	T	55	GENIC	homozygous	138004098
7	11035304	11035305	G	A	53	GENIC	homozygous	138004099
7	11035358	11035359	T	G	52	GENIC	homozygous	138004100
7	11035581	11035582	A	G	75	GENIC	possibly homozygous	138004101
7	11035878	11035879	C	T	70	GENIC	homozygous	138004102
7	11036003	11036004	C	T	66	GENIC	homozygous	138004103
7	11036448	11036449	T	C	58	GENIC	homozygous	138004104
7	11038752	11038753	G	C	53	GENIC	homozygous	138004109
7	11037131	11037132	C	T	41	GENIC	homozygous	138004105
7	11037284	11037285	G	A	39	GENIC	homozygous	138004106
7	11038423	11038424	C	T	77	GENIC	homozygous	138004107
7	11038729	11038730	A	G	54	GENIC	homozygous	138004108
7	11036218	11036220	CA		45	GENIC	homozygous	137935421
7	11034394	11034398	ATTA		51	GENIC	homozygous	137935419
7	11035869	11035870	A		65	GENIC	homozygous	137935420