chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	9000292	9000293	T		34	GENIC	homozygous	128148773
5	9000297	9000298	G	A	35	GENIC	homozygous	113639845
5	9010428	9010428		GGG	6	GENIC	homozygous	128148781
5	9010428	9010429	A	G	7	GENIC	homozygous	128279086
5	9010431	9010431		TTAGC	7	GENIC	homozygous	128148782
5	9010434	9010434		GTGGTAGAGCGCTTGCCTAGCAAGC	9	GENIC	homozygous	128148783
5	9018468	9018469	C		5	GENIC	homozygous	128148787
5	9018486	9018486		T	8	GENIC	homozygous	128148788
5	9018504	9018505	C		8	GENIC	homozygous	128148789
5	9018536	9018537	A	G	8	GENIC	homozygous	113639917
5	9018551	9018552	A		8	GENIC	homozygous	128148790
5	9018587	9018588	G		8	GENIC	homozygous	128148791
5	9018590	9018591	A		8	GENIC	homozygous	128148792
5	9021431	9021432	G	A	27	GENIC	homozygous	113639927
5	9013952	9013952		TTCTTCCCTCCCTCCCTCCCTCCCTCCCTCCTTCCCTCCCTCTCTCTTGTCTGTCTGTCTGTCCCCTTCCCTTCCCTTCCCTTCCCTTCCCCTC	7	GENIC	homozygous	130308308
5	9021401	9021402	T	C	32	GENIC	homozygous	113639925
5	9021343	9021344	C	G	32	GENIC	homozygous	130317591
5	9021450	9021451	G	A	27	GENIC	homozygous	113639929
5	9021464	9021465	A	G	23	GENIC	homozygous	114170355
5	9021602	9021603	G	C	27	GENIC	homozygous	113639931
5	9021623	9021624	T	C	26	GENIC	homozygous	113639933
5	9021631	9021632	C	T	29	GENIC	homozygous	113639935
5	9021667	9021668	G	A	27	GENIC	homozygous	113639937