chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	41774148	41774149	T	C	14	GENIC	possibly homozygous	56846648
4	41774426	41774427	C	CCCCT	2	GENIC	heterozygous	56846650
4	41774426	41774427	C	CCCT	2	GENIC	heterozygous	57725712
4	41775375	41775376	A	G	38	GENIC	heterozygous	56846652
4	41775745	41775746	C	A	14	GENIC	homozygous	56846654
4	41775762	41775763	C	CGCG	17	GENIC	homozygous	56846656
4	41775771	41775772	C	T	18	GENIC	homozygous	56846658
4	41775788	41775789	G	A	18	GENIC	homozygous	56846660
4	41775794	41775795	A	G	21	GENIC	homozygous	56846662
4	41775799	41775800	G	C	21	GENIC	homozygous	56846664
4	41775727	41775728	G	A	14	GENIC	homozygous	58064062