chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100663501	100663502	A	G	35	GENIC	homozygous	50266474
13	100663924	100663925	C	A	26	GENIC	homozygous	50266475
13	100665700	100665701	T	C	25	GENIC	homozygous	50266476
13	100665917	100665918	C	-	12	GENIC	homozygous	50266477
13	100666557	100666562	TAAAA	-----	25	GENIC	homozygous	50266478
13	100666607	100666608	G	A	29	GENIC	homozygous	50266479
13	100667964	100667965	T	G	19	GENIC	homozygous	50266480
13	100668057	100668058	T	C	25	GENIC	homozygous	50266481
13	100668414	100668417	AAA	---	17	GENIC	possibly homozygous	50266483
13	100669206	100669208	AT	--	21	GENIC	homozygous	50266484
13	100669689	100669690	G	A	18	GENIC	homozygous	50266485
13	100671308	100671309	A	-	20	GENIC	homozygous	50266486
13	100672650	100672651	A	G	24	GENIC	homozygous	50266487
13	100672745	100672746	T	TAA	22	GENIC	heterozygous	50266488
13	100672745	100672746	T	TA	22	GENIC	possibly homozygous	50266489
13	100674467	100674468	T	G	22	GENIC	homozygous	50266490
13	100674847	100674848	T	C	25	GENIC	homozygous	50266491
13	100675668	100675669	A	T	30	GENIC	homozygous	50266492
13	100678158	100678159	G	-	13	GENIC	homozygous	50266493
13	100679022	100679023	G	A	8	GENIC	homozygous	50266495
13	100664283	100664284	T	-	26	GENIC	homozygous	50201856
13	100678272	100678273	T	TA	7	GENIC	homozygous	50201858
13	100664291	100664292	T	C	29	GENIC	homozygous	50619917
13	100666564	100666565	A	T	26	GENIC	homozygous	50619918
13	100666565	100666566	C	T	26	GENIC	homozygous	50619919
13	100668429	100668430	A	G	23	GENIC	possibly homozygous	50619920