chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	58159657	58159658	A	G	10	GENIC	homozygous	53121830
8	58159661	58159662	T	C	11	GENIC	homozygous	53121831
8	58159662	58159663	G	A	11	GENIC	homozygous	53121832
8	58159758	58159759	C	T	21	GENIC	homozygous	53121833
8	58159835	58159836	C	T	21	GENIC	homozygous	53121834
8	58159860	58159861	C	T	21	GENIC	homozygous	53121835
8	58159868	58159869	C	A	27	GENIC	homozygous	53121836
8	58159874	58159875	C	T	28	GENIC	homozygous	53121837
8	58160429	58160430	C	G	24	GENIC	homozygous	53121838
8	58160622	58160623	T	G	20	GENIC	homozygous	53121839
8	58160712	58160713	G	T	47	GENIC	homozygous	53121840
8	58160877	58160878	A	G	33	GENIC	homozygous	53121841
8	58160965	58160966	T	A	25	GENIC	homozygous	53271688
8	58161054	58161055	A	G	17	GENIC	homozygous	53121842
8	58161060	58161061	C	CT	9	GENIC	homozygous	53121843
8	58161062	58161063	C	CTCCTT	13	GENIC	heterozygous	53121844