chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	80744898	80744899	A	G	45	GENIC	homozygous	46533439
18	80750171	80750172	G	A	64	GENIC	possibly homozygous	46533441
18	80750453	80750454	T	C	53	GENIC	homozygous	46533443
18	80751038	80751039	G	T	55	GENIC	possibly homozygous	46533445
18	80751788	80751789	A	G	41	GENIC	possibly homozygous	46533447
18	80752117	80752118	T	TTTTAACC	30	GENIC	homozygous	46533449
18	80752665	80752666	G	GT	61	GENIC	possibly homozygous	46533451
18	80752665	80752666	G	GTT	61	GENIC	heterozygous	46633758
18	80754090	80754091	T	C	50	GENIC	homozygous	46533455
18	80753884	80753885	C	T	69	GENIC	possibly homozygous	46533453
18	80759000	80759001	T	-	13	GENIC	possibly homozygous	46533457
18	80760486	80760487	G	T	56	GENIC	homozygous	46533459
18	80760963	80760964	A	T	73	GENIC	possibly homozygous	46533461
18	80761301	80761302	A	G	62	GENIC	homozygous	46533463
18	80768241	80768242	C	T	51	GENIC	homozygous	46533465
18	80768686	80768687	C	G	54	GENIC	possibly homozygous	46533467
18	80769326	80769327	A	C	42	GENIC	homozygous	46533469