chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	83935697	83935698	G	C	40	GENIC	homozygous	108879754
1	83936269	83936270	C	T	41	GENIC	homozygous	108879755
1	83936415	83936416	C	T	37	GENIC	homozygous	108879756
1	83936803	83936804	G	A	37	GENIC	homozygous	108879757
1	83937963	83937964	G	T	46	GENIC	homozygous	120514118
1	83937964	83937965	A	G	47	GENIC	homozygous	109304939
1	83938700	83938701	A	G	21	GENIC	homozygous	120868661
1	83938730	83938731	A	C	21	GENIC	homozygous	108879758
1	83940022	83940023	G	A	36	GENIC	homozygous	108879759
1	83940193	83940194	T	C	33	GENIC	homozygous	108879760
1	83942980	83942981	G	C	16	GENIC	homozygous	108879762
1	83943690	83943691	A	G	45	GENIC	homozygous	108879763
1	83944101	83944102	G	T	50	GENIC	possibly homozygous	108879764
1	83938413	83938414	G	T	33	GENIC	homozygous	120482416
1	83940545	83940546	T	C	33	GENIC	homozygous	120482417
1	83945166	83945167	T		46	GENIC	possibly homozygous	131259043
1	83939795	83939797	AC		26	GENIC	homozygous	131259042