chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17966838	17966839	C	A	65	GENIC	possibly homozygous	51628830
10	17967379	17967380	C	CG	54	GENIC	homozygous	51628831
10	17967392	17967393	A	-	33	GENIC	heterozygous	51335290
10	17967399	17967400	A	AC	49	GENIC	heterozygous	51628832
10	17967400	17967401	A	AC	51	GENIC	possibly homozygous	51335291
10	17967402	17967403	A	AAAC	26	GENIC	possibly homozygous	51628833
10	17967605	17967606	A	ATAACCTAGG	31	GENIC	homozygous	51335295
10	17969320	17969321	T	TA	48	GENIC	homozygous	51335300
10	17969734	17969735	G	A	91	GENIC	possibly homozygous	51628834
10	17970136	17970137	G	A	50	GENIC	homozygous	51628835
10	17970451	17970452	C	CCAAACT	19	GENIC	homozygous	51335302
10	17970570	17970571	T	TA	26	GENIC	homozygous	51335303
10	17970606	17970607	G	-	19	GENIC	homozygous	51335304
10	17970610	17970611	T	TA	18	GENIC	homozygous	51335305
10	17970615	17970616	A	-	20	GENIC	homozygous	51335306
10	17970620	17970621	T	TA	23	GENIC	homozygous	51335307
10	17971035	17971036	T	C	67	GENIC	homozygous	51335312
10	17971167	17971168	G	A	64	GENIC	homozygous	51628836
10	17971465	17971466	G	A	51	GENIC	homozygous	51628837
10	17971936	17971937	A	G	46	GENIC	homozygous	51335319
10	17971964	17971966	AA	--	36	GENIC	homozygous	51628838
10	17972145	17972147	AC	--	57	GENIC	homozygous	51335324
10	17972591	17972592	T	TA	89	GENIC	homozygous	51335329
10	17972710	17972711	C	T	83	GENIC	possibly homozygous	51628839
10	17972772	17972773	G	T	87	GENIC	homozygous	51628840
10	17972823	17972824	T	C	73	GENIC	homozygous	51335333
10	17973002	17973003	T	-	79	GENIC	homozygous	51335334
10	17973269	17973270	A	G	91	GENIC	homozygous	51628841
10	17975494	17975495	A	G	52	GENIC	homozygous	51628842