chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	111047658	111047659	C	T	52	GENIC	homozygous	143365670
7	111047699	111047700	A	C	59	GENIC	homozygous	143365671
7	111047721	111047722	A	G	58	GENIC	homozygous	143365672
7	111048322	111048323	T	C	61	GENIC	homozygous	143365673
7	111048447	111048448	G	A	70	GENIC	homozygous	145635046
7	111049215	111049216	G	A	25	GENIC	homozygous	143365674
7	111050406	111050407	G	A	55	GENIC	homozygous	143365675
7	111054810	111054811	T	C	59	GENIC	homozygous	145635047
7	111055168	111055169	C	G	43	GENIC	homozygous	143365678
7	111055308	111055309	C	T	49	GENIC	homozygous	145635048
7	111056035	111056036	T	C	32	GENIC	possibly homozygous	138182048
7	111054908	111054909	A	T	49	GENIC	homozygous	138182046
7	111055651	111055652	C	T	48	GENIC	possibly homozygous	138182047
7	111056317	111056321	AGGA		36	GENIC	homozygous	137974260
7	111054908	111054908		C	49	GENIC	homozygous	137974257
7	111055704	111055711	CTGAGCT		45	GENIC	possibly homozygous	137974258
7	111056127	111056127		A	23	GENIC	homozygous	137974259
7	111059338	111059338		CCAC	18	GENIC	possibly homozygous	137974261
7	111061639	111061640	T	A	57	GENIC	homozygous	138182049
7	111061882	111061883	T	G	62	GENIC	homozygous	138182050
7	111062830	111062831	T	C	46	GENIC	homozygous	138182051
7	111068608	111068609	C	G	30	GENIC	homozygous	138182052
7	111068725	111068726	A	C	25	GENIC	homozygous	138182053
7	111069262	111069263	A	C	41	GENIC	homozygous	138182054
7	111070627	111070628	G	A	47	GENIC	homozygous	138182055
7	111071287	111071288	C	T	66	GENIC	homozygous	138182056
7	111071306	111071307	G	A	70	GENIC	homozygous	138182057
7	111074122	111074122		CCT	50	GENIC	homozygous	137974262
7	111071820	111071821	G		22	GENIC	possibly homozygous	403617356
7	111071820	111071821	G	A	22	GENIC	heterozygous	154485231
7	111073299	111073300	T	C	61	GENIC	heterozygous	154485233
7	111073299	111073300	T		61	GENIC	homozygous	403617357
7	111073304	111073305	G		61	GENIC	homozygous	403617358
7	111073304	111073305	G	A	61	GENIC	heterozygous	403617359