chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	8999675	8999676	C	A	1	GENIC	homozygous	133670965
5	9000292	9000293	T		12	GENIC	homozygous	128148773
5	9000297	9000298	G	A	13	GENIC	homozygous	113639845
5	9007290	9007291	C	T	11	GENIC	heterozygous	114107111
5	9007295	9007296	T	C	12	GENIC	heterozygous	114107112
5	9007301	9007302	C	T	12	GENIC	heterozygous	113639876
5	9007327	9007328	C	T	12	GENIC	heterozygous	113639880
5	9007330	9007331	C	A	12	GENIC	heterozygous	113639881
5	9018486	9018486		T	1	GENIC	homozygous	128148788
5	9018504	9018505	C		1	GENIC	homozygous	128148789
5	9018551	9018552	A		1	GENIC	homozygous	128148790
5	9018587	9018588	G		1	GENIC	homozygous	128148791
5	9018590	9018591	A		1	GENIC	homozygous	128148792
5	9021431	9021432	G	A	12	GENIC	homozygous	113639927
5	9007347	9007348	C	T	13	GENIC	heterozygous	131654102
5	9007351	9007352	T	C	13	GENIC	heterozygous	113639883
5	9018536	9018537	A	G	1	GENIC	homozygous	113639917
5	9021401	9021402	T	C	12	GENIC	homozygous	113639925
5	9007347	9007347		T	12	GENIC	heterozygous	131647034
5	9021343	9021344	C	G	12	GENIC	homozygous	130317591
5	9021450	9021451	G	A	12	GENIC	homozygous	113639929
5	9021464	9021465	A	G	9	GENIC	homozygous	114170355
5	9021602	9021603	G	C	9	GENIC	homozygous	113639931
5	9021623	9021624	T	C	6	GENIC	homozygous	113639933
5	9021631	9021632	C	T	5	GENIC	homozygous	113639935
5	9021667	9021668	G	A	8	GENIC	homozygous	113639937