chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	81657676	81657677	T	A	40	GENIC	possibly homozygous	116811936
10	81657701	81657702	A	G	41	GENIC	homozygous	116811938
10	81657736	81657737	G	A	44	GENIC	homozygous	116811940
10	81658733	81658734	G	A	62	GENIC	homozygous	116811942
10	81659276	81659277	G	A	28	GENIC	possibly homozygous	116811944
10	81659280	81659281	T	C	27	GENIC	homozygous	116657318
10	81659384	81659385	T	C	41	GENIC	homozygous	116811946
10	81659507	81659508	G	A	49	GENIC	homozygous	116811948
10	81659603	81659604	G	T	40	GENIC	homozygous	116811950
10	81659609	81659610	A	T	39	GENIC	possibly homozygous	116811952
10	81660397	81660398	C	T	41	GENIC	homozygous	116811954
10	81660963	81660964	A	T	50	GENIC	homozygous	116811956
10	81661060	81661061	G	A	50	GENIC	homozygous	116811958
10	81661117	81661118	A	C	50	GENIC	possibly homozygous	116811960
10	81661157	81661158	G	A	48	GENIC	homozygous	118068872
10	81661389	81661390	A	G	54	GENIC	possibly homozygous	116811962
10	81661774	81661775	G	T	45	GENIC	homozygous	116811964
10	81661812	81661813	A	G	41	GENIC	homozygous	116811966
10	81661842	81661843	G	A	34	GENIC	homozygous	116811968
10	81662190	81662191	C	T	50	GENIC	homozygous	116811970
10	81662601	81662602	G	A	40	GENIC	homozygous	116811972
10	81662641	81662642	G	A	38	GENIC	homozygous	116811974
10	81662934	81662935	A	T	24	GENIC	homozygous	117179833
10	81663244	81663245	A	G	45	GENIC	homozygous	116811976
10	81663507	81663508	T	C	52	GENIC	homozygous	116811978
10	81663847	81663848	T	C	52	GENIC	homozygous	116811980
10	81664113	81664114	T	C	42	GENIC	homozygous	116657326
10	81664548	81664549	G	A	78	GENIC	homozygous	116811982
10	81665699	81665700	A	G	51	GENIC	homozygous	116657328
10	81665895	81665896	G	A	78	GENIC	homozygous	116811984
10	81666469	81666470	T	C	52	GENIC	homozygous	116657330
10	81660129	81660130	A	G	36	GENIC	homozygous	116897938