chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17967402	17967403	A	AAAC	29	GENIC	possibly homozygous	51628833
10	17967605	17967606	A	ATAACCTAGG	18	GENIC	homozygous	51335295
10	17968746	17968747	G	A	33	GENIC	homozygous	51815629
10	17969320	17969321	T	TAA	34	GENIC	homozygous	51815631
10	17969656	17969657	T	C	50	GENIC	possibly homozygous	51815633
10	17969708	17969709	A	C	41	GENIC	possibly homozygous	51815635
10	17970451	17970452	C	CCAAACT	19	GENIC	homozygous	51335302
10	17970570	17970571	T	TA	23	GENIC	homozygous	51335303
10	17970606	17970607	G	-	24	GENIC	homozygous	51335304
10	17970610	17970611	T	TA	25	GENIC	homozygous	51335305
10	17970615	17970616	A	-	20	GENIC	homozygous	51335306
10	17970620	17970621	T	TA	20	GENIC	homozygous	51335307
10	17971035	17971036	T	C	40	GENIC	homozygous	51335312
10	17971399	17971400	A	AT	20	GENIC	heterozygous	51335315
10	17971409	17971410	C	T	41	GENIC	homozygous	51815637
10	17971850	17971851	C	T	53	GENIC	homozygous	51815639
10	17971936	17971937	A	G	25	GENIC	possibly homozygous	51335319
10	17971963	17971964	C	CA	8	GENIC	heterozygous	51815641
10	17972145	17972147	AC	--	22	GENIC	homozygous	51335324
10	17972342	17972343	A	C	38	GENIC	possibly homozygous	51815643
10	17972591	17972592	T	TA	46	GENIC	homozygous	51335329
10	17972823	17972824	T	C	57	GENIC	homozygous	51335333
10	17973002	17973003	T	-	46	GENIC	homozygous	51335334
10	17974411	17974412	G	A	51	GENIC	homozygous	51815645
10	17975494	17975495	A	G	27	GENIC	homozygous	51628842