chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	39610360	39610361	C	CGA	12	GENIC	heterozygous	50742454
11	39611466	39611468	GT	--	9	GENIC	heterozygous	51260161
11	39612720	39612722	TG	--	1	GENIC	homozygous	50742461
11	39617572	39617573	G	A	32	GENIC	homozygous	50742472
11	39619448	39619449	A	G	28	GENIC	homozygous	50742474
11	39619484	39619485	A	C	25	GENIC	homozygous	50742475
11	39619777	39619778	A	T	37	GENIC	homozygous	50742476
11	39619813	39619814	C	T	38	GENIC	homozygous	50742477
11	39619827	39619828	A	G	38	GENIC	homozygous	50742478
11	39619855	39619856	T	G	39	GENIC	homozygous	50742479
11	39620251	39620252	T	C	38	GENIC	homozygous	50742480
11	39620281	39620282	A	T	36	GENIC	homozygous	50742481
11	39620738	39620739	C	T	27	GENIC	homozygous	51585976
11	39620904	39620905	A	G	17	GENIC	homozygous	50742482
11	39620998	39620999	G	T	25	GENIC	homozygous	51585978
11	39621191	39621192	A	G	18	GENIC	homozygous	50742483
11	39621358	39621359	G	A	17	GENIC	homozygous	50742484
11	39621538	39621539	G	A	12	GENIC	homozygous	50742485
11	39621862	39621863	G	A	20	GENIC	homozygous	51585980
11	39622214	39622215	T	G	22	GENIC	homozygous	50742487
11	39622216	39622217	G	A	23	GENIC	homozygous	50742488
11	39622412	39622413	T	C	19	GENIC	homozygous	50742489
11	39622418	39622419	T	A	19	GENIC	homozygous	50742490
11	39622507	39622508	T	TG	17	GENIC	homozygous	51585982
11	39622536	39622539	TGT	---	16	GENIC	homozygous	50742491
11	39622602	39622603	A	AT	22	GENIC	homozygous	50742492
11	39622660	39622661	T	C	27	GENIC	homozygous	50742493
11	39622794	39622795	G	A	34	GENIC	homozygous	50742494
11	39623145	39623146	C	T	13	GENIC	homozygous	50742495
11	39623448	39623449	C	T	15	GENIC	homozygous	50742496
11	39623586	39623587	A	T	33	GENIC	homozygous	50742497
11	39623593	39623594	A	G	32	GENIC	homozygous	50742498