chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	38233976	38233978	AA		52	GENIC	homozygous	128023469
4	38234192	38234193	A		46	GENIC	homozygous	128023470
4	38234198	38234199	A	G	45	GENIC	homozygous	112591155
4	38234336	38234337	A	T	53	GENIC	homozygous	112591157
4	38234353	38234354	T		52	GENIC	homozygous	128023471
4	38234403	38234404	C	T	45	GENIC	homozygous	112591159
4	38234720	38234721	A	G	44	GENIC	homozygous	112591161
4	38234768	38234769	G	T	39	GENIC	homozygous	112591163
4	38235023	38235024	T	A	50	GENIC	homozygous	112591165
4	38235188	38235189	T	G	45	GENIC	homozygous	112591167
4	38235222	38235223	A	T	52	GENIC	homozygous	112591169
4	38235541	38235542	C	T	41	GENIC	homozygous	112591171
4	38235696	38235697	G	C	42	GENIC	homozygous	112591173
4	38236962	38236963	C	T	47	GENIC	homozygous	112591175
4	38237357	38237358	T	C	47	GENIC	homozygous	112591177
4	38237769	38237770	G	A	49	GENIC	homozygous	112591179
4	38238758	38238759	G	A	37	GENIC	homozygous	112591181
4	38238855	38238856	G	A	46	GENIC	homozygous	112591183
4	38240660	38240661	C	G	37	GENIC	homozygous	112591185