chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	39608330	39608331	C	-	10	GENIC	heterozygous	51181009
11	39609051	39609052	G	A	13	GENIC	homozygous	51160666
11	39609179	39609180	T	C	20	GENIC	homozygous	50742449
11	39609351	39609352	T	C	26	GENIC	possibly homozygous	50742450
11	39609493	39609494	T	C	12	GENIC	possibly homozygous	50742452
11	39610747	39610748	G	A	18	GENIC	homozygous	50742456
11	39611856	39611857	G	A	13	GENIC	heterozygous	50742459
11	39612303	39612304	C	A	20	GENIC	possibly homozygous	51160668
11	39612401	39612402	G	A	11	GENIC	homozygous	50742460
11	39612884	39612885	A	G	17	GENIC	homozygous	50742462
11	39614047	39614048	A	C	14	GENIC	heterozygous	50742464
11	39614386	39614387	A	G	30	GENIC	homozygous	50742466
11	39614493	39614494	C	A	5	GENIC	heterozygous	50742467
11	39617572	39617573	G	A	33	GENIC	possibly homozygous	50742472
11	39617647	39617648	G	C	19	GENIC	possibly homozygous	50742473
11	39617842	39617843	G	A	8	GENIC	heterozygous	51160670
11	39619484	39619485	A	C	15	GENIC	homozygous	50742475
11	39619827	39619828	A	G	17	GENIC	possibly homozygous	50742478
11	39620251	39620252	T	C	23	GENIC	possibly homozygous	50742480
11	39620398	39620399	T	C	18	GENIC	homozygous	51486905
11	39620769	39620770	A	G	7	GENIC	homozygous	51486907
11	39621191	39621192	A	G	9	GENIC	heterozygous	50742483
11	39622412	39622413	T	C	13	GENIC	homozygous	50742489
11	39622418	39622419	T	A	13	GENIC	homozygous	50742490
11	39622536	39622539	TGT	---	6	GENIC	homozygous	50742491
11	39622602	39622603	A	AT	16	GENIC	heterozygous	50742492
11	39622660	39622661	T	C	14	GENIC	possibly homozygous	50742493
11	39623593	39623594	A	G	2	GENIC	homozygous	50742498