chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	9675786	9675866	ACAGACACACACACACTCACAGACACACAGATACACACACACACTCACAGAAACACAGATACACACACAGACACTCACAT		19	GENIC	homozygous	147550064
7	9676090	9676091	A	T	13	GENIC	homozygous	147551530
7	9676107	9676108	G	C	14	GENIC	homozygous	147551531
7	9676117	9676151	CACACAGACACACAGATACAGACGCACACACACT		13	GENIC	homozygous	147550065
7	9676290	9676291	T	A	14	GENIC	possibly homozygous	147551532
7	9676316	9676317	G	A	17	GENIC	possibly homozygous	147551536
7	9676294	9676295	A	T	15	GENIC	possibly homozygous	147551533
7	9676301	9676302	C	A	16	GENIC	possibly homozygous	147551534
7	9676313	9676314	G	C	18	GENIC	possibly homozygous	147551535
7	9676321	9676322	C	G	18	GENIC	possibly homozygous	147551537
7	9676558	9676558		ACAGACACACACACACAGACACACACAT	17	GENIC	heterozygous	147550066
7	9676671	9676679	CACAGACA		29	GENIC	homozygous	147550067
7	9681150	9681151	C	A	61	GENIC	possibly homozygous	147551538
7	9684140	9684148	GACTCCCA		41	GENIC	homozygous	147550068
7	9684589	9684592	CAT		57	GENIC	homozygous	147550069
7	9690006	9690007	A	G	50	GENIC	homozygous	138000420
7	9690262	9690263	T	C	62	GENIC	homozygous	138000422