chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	108746464	108746465	A	G	15	GENIC	homozygous	116636614
8	108752073	108752074	C	T	10	GENIC	homozygous	116636620
8	108753065	108753066	T	C	20	GENIC	homozygous	116636626
8	108755486	108755487	A	G	20	GENIC	homozygous	116636628
8	108768715	108768716	C	T	37	GENIC	homozygous	116636634
8	108769243	108769244	T	C	22	GENIC	homozygous	116636636
8	108769255	108769256	A	G	22	GENIC	homozygous	116636638
8	108769729	108769730	A	G	11	GENIC	homozygous	116636640
8	108770010	108770011	C	T	6	GENIC	homozygous	116636642
8	108770235	108770236	T	G	17	GENIC	homozygous	116636644
8	108770900	108770901	C	G	25	GENIC	homozygous	116636646
8	108771167	108771168	C	T	34	GENIC	homozygous	116636648
8	108771441	108771442	G	A	28	GENIC	homozygous	116636650
8	108771454	108771455	A	C	32	GENIC	homozygous	116636652
8	108771794	108771795	C	T	25	GENIC	homozygous	116636654
8	108771899	108771900	A	T	20	GENIC	homozygous	116636656
8	108772603	108772604	A	G	21	GENIC	homozygous	116636660
8	108773219	108773220	G	A	20	GENIC	homozygous	116636662
8	108773632	108773633	G	A	20	GENIC	homozygous	116636664
8	108774411	108774412	G	C	19	GENIC	homozygous	116636668
8	108774645	108774646	A	G	25	GENIC	homozygous	116636670
8	108774749	108774750	T	C	10	GENIC	homozygous	116636672
8	108775215	108775216	C	T	19	GENIC	homozygous	116636674
8	108776221	108776222	C	T	10	GENIC	homozygous	116636682
8	108776983	108776984	T	C	21	GENIC	homozygous	116636684
8	108777010	108777011	T	C	17	GENIC	homozygous	116636686
8	108777182	108777183	G	T	11	GENIC	homozygous	116636688
8	108778179	108778180	T	G	10	GENIC	homozygous	116636690
8	108778413	108778414	A	C	26	GENIC	homozygous	116636692