chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11038298	11038299	A	G	35	GENIC	homozygous	139082976
12	11039168	11039169	G	A	29	GENIC	homozygous	139082978
12	11044296	11044296		C	53	GENIC	homozygous	139040630
12	11049131	11049132	T	C	43	GENIC	homozygous	139082983
12	11050334	11050335	C	T	44	GENIC	homozygous	139082984
12	11050502	11050503	A	T	53	GENIC	homozygous	139082985
12	11050939	11050940	G	A	51	GENIC	homozygous	139082986
12	11052007	11052008	C	T	47	GENIC	homozygous	139082987
12	11052801	11052802	C	T	33	GENIC	possibly homozygous	143528515
12	11043144	11043145	A	G	41	GENIC	homozygous	143528510
12	11045209	11045210	G	A	39	GENIC	homozygous	143528511
12	11045276	11045277	C	T	37	GENIC	homozygous	143528512
12	11048411	11048412	G	A	48	GENIC	homozygous	143528513
12	11052396	11052397	A	G	60	GENIC	possibly homozygous	143528514
12	11051925	11051925		GGTGTG	36	GENIC	homozygous	143519517
12	11052918	11052918		CTGGAACTCAAAGTTTACC	42	GENIC	homozygous	139040632
12	11053420	11053421	G	C	34	GENIC	homozygous	143528516
12	11053841	11053842	C	T	56	GENIC	homozygous	139082990
12	11054011	11054012	T	A	38	GENIC	homozygous	143528517
12	11055870	11055871	C	T	45	GENIC	homozygous	139082992