chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	56266522	56266523	G	GCACACTGC	31	GENIC	homozygous	46468927
18	56267617	56267618	C	CAG	30	GENIC	homozygous	46468929
18	56268209	56268210	G	A	65	GENIC	possibly homozygous	46468931
18	56268777	56268778	A	G	69	GENIC	homozygous	46468933
18	56270448	56270449	A	G	30	GENIC	possibly homozygous	46468935
18	56271355	56271356	G	A	32	GENIC	homozygous	46468937
18	56271404	56271405	C	T	40	GENIC	homozygous	46468939
18	56271463	56271464	A	G	41	GENIC	homozygous	46468941
18	56271524	56271525	T	A	46	GENIC	homozygous	46468943
18	56271583	56271584	T	A	53	GENIC	possibly homozygous	46468945
18	56271646	56271647	T	TC	35	GENIC	homozygous	46468947
18	56271686	56271687	A	T	17	GENIC	heterozygous	46468949
18	56271693	56271694	T	TA	16	GENIC	possibly homozygous	46468951
18	56271707	56271708	A	T	18	GENIC	homozygous	46468953
18	56271756	56271757	T	-	26	GENIC	homozygous	46468955
18	56271761	56271762	T	A	27	GENIC	heterozygous	46468957
18	56271771	56271772	C	-	28	GENIC	homozygous	46468959
18	56273693	56273694	G	A	43	GENIC	homozygous	46468961
18	56274098	56274099	C	T	48	GENIC	homozygous	46468963
18	56274740	56274741	T	A	37	GENIC	homozygous	46468965
18	56275136	56275137	C	T	32	GENIC	homozygous	46468967
18	56275406	56275407	C	G	57	GENIC	homozygous	46468969
18	56275934	56275935	C	A	48	GENIC	homozygous	46468971
18	56276087	56276088	G	A	51	GENIC	homozygous	46468973
18	56276116	56276117	T	C	40	GENIC	homozygous	46468975
18	56276174	56276175	C	T	37	GENIC	homozygous	46468977
18	56276499	56276500	A	G	28	GENIC	homozygous	46468979
18	56276691	56276692	A	-	7	GENIC	homozygous	46468981
18	56276930	56276931	A	G	47	GENIC	possibly homozygous	46468983
18	56277746	56277747	T	TA	19	GENIC	homozygous	46468985
18	56277825	56277826	C	T	28	GENIC	homozygous	46468987