chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11038298	11038299	A	G	41	GENIC	homozygous	139082976
12	11039013	11039014	T		43	GENIC	homozygous	139040629
12	11039168	11039169	G	A	40	GENIC	homozygous	139082978
12	11039906	11039907	G	A	49	GENIC	homozygous	144919201
12	11044296	11044296		C	62	GENIC	homozygous	139040630
12	11050502	11050503	A	T	51	GENIC	homozygous	139082985
12	11043358	11043359	G	A	50	GENIC	homozygous	139082980
12	11044868	11044869	G	C	49	GENIC	homozygous	139082981
12	11045142	11045143	A	C	47	GENIC	homozygous	144919202
12	11049131	11049132	T	C	48	GENIC	homozygous	139082983
12	11050334	11050335	C	T	46	GENIC	homozygous	139082984
12	11041622	11041626	TGTA		14	GENIC	homozygous	144913194
12	11041592	11041592		TATTATTTTTTTAA	19	GENIC	heterozygous	145150797
12	11041602	11041603	G	A	13	GENIC	heterozygous	148929194
12	11050939	11050940	G	A	58	GENIC	homozygous	139082986
12	11052007	11052008	C	T	50	GENIC	homozygous	139082987
12	11052918	11052918		CTGGAACTCAAAGTTTACC	34	GENIC	homozygous	139040632
12	11053841	11053842	C	T	43	GENIC	homozygous	139082990
12	11055870	11055871	C	T	46	GENIC	homozygous	139082992
12	11055975	11055976	G	A	46	GENIC	homozygous	139082993