chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11038298	11038299	A	G	31	GENIC	homozygous	139082976
12	11038955	11038956	G	T	20	GENIC	homozygous	139082977
12	11039013	11039014	T		24	GENIC	possibly homozygous	139040629
12	11039168	11039169	G	A	19	GENIC	homozygous	139082978
12	11039411	11039412	T	A	22	GENIC	homozygous	139082979
12	11043358	11043359	G	A	21	GENIC	homozygous	139082980
12	11044296	11044296		C	34	GENIC	homozygous	139040630
12	11044868	11044869	G	C	29	GENIC	homozygous	139082981
12	11046308	11046309	T	C	17	GENIC	homozygous	139082982
12	11049131	11049132	T	C	30	GENIC	homozygous	139082983
12	11049659	11049659		GCTCA	19	GENIC	homozygous	139040631
12	11050334	11050335	C	T	24	GENIC	homozygous	139082984
12	11050502	11050503	A	T	25	GENIC	homozygous	139082985
12	11050939	11050940	G	A	18	GENIC	homozygous	139082986
12	11052007	11052008	C	T	19	GENIC	homozygous	139082987
12	11052224	11052225	T	G	31	GENIC	homozygous	139082988
12	11052366	11052367	C	G	26	GENIC	homozygous	139082989
12	11052918	11052918		CTGGAACTCAAAGTTTACC	23	GENIC	homozygous	139040632
12	11053841	11053842	C	T	27	GENIC	homozygous	139082990
12	11054299	11054300	C	T	28	GENIC	homozygous	139082991
12	11055870	11055871	C	T	29	GENIC	homozygous	139082992
12	11055975	11055976	G	A	24	GENIC	homozygous	139082993