chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84517834	84517835	G	A	40	GENIC	homozygous	116069984
11	84518598	84518599	T	C	19	GENIC	heterozygous	118210306
11	84518727	84518728	C	T	65	GENIC	heterozygous	118210307
11	84519104	84519105	C	A	41	GENIC	homozygous	116069986
11	84519328	84519329	C	T	41	GENIC	homozygous	116069988
11	84519898	84519899	A	G	39	GENIC	homozygous	116069990
11	84520804	84520805	G	T	36	GENIC	homozygous	116069992
11	84523429	84523430	T	A	71	GENIC	heterozygous	118210308
11	84523431	84523432	A	T	72	GENIC	heterozygous	118210309
11	84524100	84524101	A	G	23	GENIC	possibly homozygous	118210310
11	84524571	84524572	T	C	56	GENIC	heterozygous	118187633
11	84526819	84526820	A	T	34	GENIC	homozygous	116069994
11	84533447	84533448	C	G	28	GENIC	homozygous	116162581
11	84534682	84534683	C	T	33	GENIC	homozygous	116069996
11	84535321	84535322	C	T	31	GENIC	homozygous	116069998
11	84536189	84536190	T	C	42	GENIC	homozygous	116070000
11	84538326	84538327	T	C	43	GENIC	homozygous	116070002
11	84539458	84539459	C	A	34	GENIC	homozygous	116070004
11	84539702	84539703	G	A	32	GENIC	homozygous	116070006
11	84540052	84540053	C	T	36	GENIC	possibly homozygous	116207839
11	84542020	84542021	T	C	35	GENIC	possibly homozygous	116070010
11	84540302	84540303	T	C	38	GENIC	homozygous	116070008