chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	109817557	109817558	T	C	47	GENIC	homozygous	148690236
3	109817795	109817795		T	56	GENIC	homozygous	146696758
3	109818514	109818515	T	A	39	GENIC	homozygous	146719733
3	109818972	109818974	TG		41	GENIC	homozygous	136583637
3	109823455	109823455		AATA	21	GENIC	homozygous	148683019
3	109823623	109823624	G	T	36	GENIC	homozygous	148690237
3	109823702	109823702		CTTCAGCGT	21	GENIC	homozygous	148683020
3	109824126	109824132	TCTCTG		7	GENIC	homozygous	148683021
3	109824274	109824275	A	T	41	GENIC	homozygous	148690238
3	109824398	109824399	C	T	41	GENIC	homozygous	148690239
3	109824586	109824587	T	C	49	GENIC	homozygous	141529370
3	109824979	109824980	A	G	46	GENIC	homozygous	141529371
3	109826466	109826467	C	T	49	GENIC	homozygous	148690240