chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	56059777	56059778	T	C	9	GENIC	homozygous	111577719
3	56059864	56059865	A	G	16	GENIC	homozygous	111577720
3	56060071	56060072	C	A	5	GENIC	homozygous	111577721
3	56060315	56060316	C	T	12	GENIC	homozygous	111577722
3	56060318	56060319	G	A	12	GENIC	homozygous	111577723
3	56060330	56060331	C	T	10	GENIC	homozygous	111577724
3	56060592	56060593	G	A	8	GENIC	homozygous	111577725
3	56062332	56062333	C	G	11	GENIC	homozygous	111577726
3	56062805	56062806	T	C	10	GENIC	homozygous	111577727
3	56063966	56063967	C	G	8	GENIC	homozygous	111577728
3	56064193	56064194	G	A	8	GENIC	homozygous	111577729
3	56064916	56064917	A	G	14	GENIC	possibly homozygous	111577730
3	56065573	56065574	G	A	5	GENIC	homozygous	111577733
3	56066977	56066978	T	C	11	GENIC	homozygous	111577734
3	56067902	56067903	G	A	20	GENIC	homozygous	111577735
3	56068701	56068702	A	G	12	GENIC	homozygous	111577736
3	56068941	56068942	T	C	4	GENIC	homozygous	111577737
3	56069123	56069124	G	A	13	GENIC	homozygous	111577738
3	56069609	56069610	T	C	7	GENIC	homozygous	111577739
3	56070131	56070132	G	A	9	GENIC	homozygous	111577740
3	56070257	56070258	G	T	7	GENIC	homozygous	111577741