chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	71750784	71750785	T	C	27	GENIC	homozygous	112707096
4	71750806	71750807	G	A	30	GENIC	homozygous	119512291
4	71751533	71751534	C	G	21	GENIC	homozygous	119512293
4	71752448	71752449	C	T	24	GENIC	homozygous	113033497
4	71756491	71756492	C	T	24	GENIC	homozygous	113033501
4	71756640	71756641	C	T	22	GENIC	homozygous	119512295
4	71757500	71757501	C	T	22	GENIC	homozygous	119512297
4	71759188	71759189	C	T	21	GENIC	homozygous	113033503
4	71759784	71759785	C	T	19	GENIC	homozygous	113033504
4	71760197	71760198	G	A	20	GENIC	homozygous	113033505
4	71761014	71761015	G	T	21	GENIC	homozygous	119512299
4	71762317	71762318	T	C	19	GENIC	homozygous	113033506
4	71762349	71762350	C	T	17	GENIC	homozygous	113033507
4	71763046	71763047	A	G	26	GENIC	homozygous	112707102
4	71763637	71763638	T	C	13	GENIC	homozygous	113033508
4	71761138	71761138		GAA	21	GENIC	homozygous	131353267