chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	116928822	116928823	A	C	38	GENIC	homozygous	115845859
7	116930571	116930572	T	C	69	GENIC	homozygous	115845861
7	116930772	116930773	T		43	GENIC	possibly homozygous	128510394
7	116930950	116930951	T	C	54	GENIC	homozygous	115845863
7	116931640	116931641	T	C	44	GENIC	homozygous	115845865
7	116932522	116932523	G	A	64	GENIC	homozygous	115845867
7	116932532	116932533	G	A	64	GENIC	homozygous	115845869
7	116933057	116933058	A	T	64	GENIC	homozygous	115845871
7	116933972	116933973	A	G	51	GENIC	homozygous	115845873
7	116934411	116934412	G	A	52	GENIC	homozygous	115845875
7	116935780	116935781	G	T	57	GENIC	homozygous	115845877
7	116937285	116937286	G	T	55	GENIC	homozygous	115845879
7	116939505	116939505		CTG	64	GENIC	homozygous	128510395
7	116939739	116939740	T	G	69	GENIC	homozygous	115845881
7	116941317	116941318	T	C	54	GENIC	homozygous	115845883
7	116941522	116941523	A	G	54	GENIC	homozygous	115845885
7	116941528	116941529	T	A	51	GENIC	homozygous	115845887
7	116941529	116941530	C	A	51	GENIC	homozygous	115845889
7	116941685	116941686	A		60	GENIC	homozygous	128510396
7	116941720	116941721	C	A	56	GENIC	homozygous	115845891
7	116941721	116941722	T	G	56	GENIC	homozygous	115845893