chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	111210273	111210274	G	C	29	GENIC	homozygous	116646901
8	111210543	111210544	C	A	34	GENIC	homozygous	116646903
8	111210843	111210844	C	G	25	GENIC	homozygous	116646905
8	111211165	111211166	A	G	28	GENIC	homozygous	116646907
8	111211283	111211284	A	C	29	GENIC	homozygous	116646909
8	111211492	111211493	C	T	50	GENIC	homozygous	116646911
8	111211541	111211542	C	T	46	GENIC	homozygous	116646913
8	111212063	111212064	T	C	30	GENIC	homozygous	116646915
8	111212361	111212362	C	T	38	GENIC	homozygous	116646917
8	111213706	111213707	G	A	35	GENIC	homozygous	116646919
8	111215850	111215851	G	T	24	GENIC	homozygous	116646921
8	111218983	111218984	G	A	21	GENIC	homozygous	116646923
8	111220405	111220406	G	A	49	GENIC	homozygous	116986961
8	111220661	111220662	A	G	43	GENIC	homozygous	116646925
8	111221039	111221040	A	G	22	GENIC	homozygous	116646927
8	111221209	111221210	C	T	31	GENIC	homozygous	116646929
8	111221253	111221254	C	G	33	GENIC	homozygous	116646931
8	111221256	111221257	A	G	33	GENIC	homozygous	116646933
8	111222277	111222278	G	C	28	GENIC	homozygous	116646935
8	111222759	111222760	T	C	28	GENIC	homozygous	116646937