chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84041901	84041902	G	A	68	GENIC	homozygous	116069066
11	84042146	84042147	A	G	40	GENIC	homozygous	116069068
11	84042198	84042199	A	G	39	GENIC	homozygous	116069071
11	84042507	84042508	T	C	34	GENIC	homozygous	118210161
11	84043119	84043120	C	T	40	GENIC	possibly homozygous	116069073
11	84043127	84043128	C	T	41	GENIC	homozygous	116069075
11	84043941	84043942	A	G	15	GENIC	homozygous	116207739
11	84044072	84044073	G	A	28	GENIC	homozygous	116069077
11	84044170	84044171	G	C	45	GENIC	possibly homozygous	116069079
11	84044171	84044172	G	C	48	GENIC	homozygous	116069081
11	84044202	84044203	C	G	56	GENIC	homozygous	116069083
11	84044934	84044935	T	A	51	GENIC	possibly homozygous	116069085
11	84045112	84045113	G	C	41	GENIC	homozygous	116069087
11	84046037	84046038	A	G	50	GENIC	homozygous	116069089
11	84046183	84046184	T	G	53	GENIC	homozygous	116069091
11	84046487	84046488	C	T	48	GENIC	homozygous	116069093
11	84047391	84047392	C	T	41	GENIC	homozygous	116069095
11	84047408	84047409	C	G	41	GENIC	homozygous	116207745