chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80639008	80639009	G	A	14	GENIC	homozygous	118209551
11	80639272	80639273	G	C	10	GENIC	homozygous	116064503
11	80639435	80639436	C	T	17	GENIC	homozygous	118199951
11	80639727	80639728	A	G	21	GENIC	homozygous	116064513
11	80640211	80640212	T	C	17	GENIC	homozygous	116064523
11	80640490	80640491	C	T	14	GENIC	homozygous	116064527
11	80640743	80640744	C	G	19	GENIC	homozygous	116309917
11	80640796	80640797	G	A	4	GENIC	homozygous	116064533
11	80641045	80641046	A	G	21	GENIC	homozygous	116064541
11	80641815	80641816	T	C	20	GENIC	homozygous	116064545
11	80642035	80642036	A	G	15	GENIC	homozygous	116309918
11	80642307	80642308	T	A	13	GENIC	homozygous	116309919
11	80642711	80642712	C	T	21	GENIC	homozygous	116309920
11	80644189	80644190	C	T	15	GENIC	homozygous	118209553
11	80644512	80644513	A	G	14	GENIC	homozygous	118209554
11	80644925	80644926	A	G	17	GENIC	homozygous	116064583
11	80645081	80645082	A	C	13	GENIC	homozygous	116064587
11	80646346	80646347	G	C	30	GENIC	homozygous	118209555
11	80647485	80647486	A	G	16	GENIC	homozygous	116064629
11	80650723	80650724	A	G	20	GENIC	homozygous	118209556