chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	17880825	17880826	T	G	15	GENIC	homozygous	110453771
18	17882152	17882153	G	T	26	GENIC	homozygous	110289765
18	17882345	17882346	C	G	27	GENIC	homozygous	110453772
18	17886363	17886364	A	G	23	GENIC	homozygous	110453773
18	17886611	17886612	A	G	40	GENIC	homozygous	110453774
18	17886795	17886796	T	G	31	GENIC	homozygous	110453775
18	17886932	17886933	C	T	13	GENIC	homozygous	110453776
18	17891956	17891957	C	T	28	GENIC	homozygous	110289769
18	17892931	17892932	C	T	28	GENIC	homozygous	110453778
18	17893015	17893016	C	T	23	GENIC	homozygous	110289771
18	17893498	17893499	C	G	17	GENIC	homozygous	110289773
18	17893671	17893672	T	C	33	GENIC	homozygous	110289775
18	17893809	17893810	T	C	31	GENIC	homozygous	110453779
18	17894228	17894229	A	C	28	GENIC	homozygous	110453780
18	17894361	17894362	A	C	49	GENIC	homozygous	110453781
18	17898015	17898016	G	A	13	GENIC	homozygous	110453782
18	17899093	17899094	G	A	43	GENIC	homozygous	110453785
18	17899167	17899168	C	T	35	GENIC	homozygous	110453786
18	17900902	17900903	T	C	30	GENIC	homozygous	110289799
18	17901747	17901748	T	G	26	GENIC	homozygous	110289801
18	17901914	17901915	T	G	20	GENIC	homozygous	110453787
18	17902961	17902962	T	A	19	GENIC	homozygous	110453788
18	17903599	17903600	A	T	16	GENIC	homozygous	110289807
18	17903607	17903608	T	C	13	GENIC	homozygous	110453789
18	17903730	17903731	G	A	18	GENIC	homozygous	110289813
18	17901345	17901346	C	T	28	GENIC	homozygous	110528094
18	17904251	17904252	G	A	14	GENIC	homozygous	110528096
18	17909739	17909740	G	A	29	GENIC	homozygous	110528098