chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	84139573	84139574	G	T	37	GENIC	homozygous	139031948
11	84139762	84139763	A	G	37	GENIC	homozygous	139031949
11	84139920	84139921	A		44	GENIC	homozygous	138898130
11	84140014	84140015	G	A	43	GENIC	homozygous	139031950
11	84140077	84140084	TGGGTCC		25	GENIC	homozygous	138898131
11	84140252	84140253	C	T	35	GENIC	homozygous	139031951
11	84140314	84140315	C	T	38	GENIC	homozygous	139031952
11	84140401	84140402	T	A	49	GENIC	homozygous	139031953
11	84140414	84140415	A	G	51	GENIC	homozygous	139031954
11	84140652	84140653	C	T	36	GENIC	homozygous	139031955
11	84140681	84140682	G	A	36	GENIC	homozygous	139031956
11	84140962	84140962		A	28	GENIC	homozygous	138898132
11	84140978	84140979	G	A	28	GENIC	homozygous	139031957
11	84141029	84141030	C	T	30	GENIC	homozygous	139031958
11	84141080	84141081	C	T	36	GENIC	homozygous	139031959
11	84142000	84142001	A	G	43	GENIC	homozygous	139031960
11	84142111	84142112	G	A	35	GENIC	homozygous	139031961
11	84140078	84140079	G		25	GENIC	homozygous	403902879
11	84140078	84140079	G	A	25	GENIC	heterozygous	154725085