chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17966832	17966833	T	TC	23	GENIC	homozygous	52117677
10	17967379	17967380	C	CG	11	GENIC	homozygous	51628831
10	17967399	17967400	A	AC	11	GENIC	possibly homozygous	51628832
10	17967400	17967401	A	AC	4	GENIC	heterozygous	51335291
10	17967402	17967403	A	AAAC	7	GENIC	homozygous	51628833
10	17967605	17967606	A	ATAACCTAGG	9	GENIC	homozygous	51335295
10	17968750	17968751	T	TA	25	GENIC	homozygous	52117679
10	17969320	17969321	T	TA	14	GENIC	homozygous	51335300
10	17969734	17969735	G	A	29	GENIC	homozygous	51628834
10	17970451	17970452	C	CCAAACT	8	GENIC	homozygous	51335302
10	17970570	17970571	T	TA	13	GENIC	homozygous	51335303
10	17970606	17970607	G	-	8	GENIC	homozygous	51335304
10	17970610	17970611	T	TA	7	GENIC	homozygous	51335305
10	17970615	17970616	A	-	8	GENIC	homozygous	51335306
10	17970620	17970621	T	TA	8	GENIC	homozygous	51335307
10	17971035	17971036	T	C	11	GENIC	homozygous	51335312
10	17971167	17971168	G	A	17	GENIC	homozygous	51628836
10	17971465	17971466	G	A	23	GENIC	homozygous	51628837
10	17971936	17971937	A	G	30	GENIC	homozygous	51335319
10	17972145	17972147	AC	--	10	GENIC	homozygous	51335324
10	17972591	17972592	T	TA	15	GENIC	homozygous	51335329
10	17972772	17972773	G	T	13	GENIC	homozygous	51628840
10	17972823	17972824	T	C	15	GENIC	homozygous	51335333
10	17973002	17973003	T	-	18	GENIC	possibly homozygous	51335334
10	17973269	17973270	A	G	21	GENIC	homozygous	51628841
10	17975494	17975495	A	G	39	GENIC	homozygous	51628842