chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	243354543	243354544	C	A	44	GENIC	homozygous	135852702
1	243354766	243354767	G	A	39	GENIC	homozygous	135852703
1	243354777	243354778	C	T	42	GENIC	homozygous	135852704
1	243355087	243355088	A	C	43	GENIC	homozygous	141305557
1	243357035	243357036	G	C	52	GENIC	homozygous	141305558
1	243358061	243358062	T	C	32	GENIC	homozygous	135852706
1	243358286	243358286		CCT	13	GENIC	homozygous	135469783
1	243358364	243358365	T	C	9	GENIC	homozygous	135852707
1	243358904	243358905	G	A	34	GENIC	homozygous	141305559
1	243358971	243358972	A	C	27	GENIC	homozygous	141305560
1	243359350	243359351	A	G	45	GENIC	homozygous	135852708
1	243359797	243359798	G	A	58	GENIC	homozygous	141305561
1	243360762	243360763	T	C	46	GENIC	homozygous	135852710
1	243361243	243361244	G	A	36	GENIC	homozygous	135852711
1	243362637	243362638	A	G	41	GENIC	homozygous	135852712
1	243368341	243368353	TGTGTGTGTGTT		30	GENIC	homozygous	144530219
1	243358340	243358346	CTCCTC		6	GENIC	homozygous	141181114
1	243358649	243358649		CCTCCTCCTCCTCCC	1	GENIC	homozygous	141181115
1	243365432	243365433	A	T	14	GENIC	homozygous	144574298
1	243365433	243365434	T	C	14	GENIC	homozygous	144574299