chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	113834036	113834037	A	C	17	GENIC	homozygous	54228868
7	113834739	113834740	G	A	12	GENIC	possibly homozygous	54228870
7	113836882	113836883	C	T	13	GENIC	homozygous	54228872
7	113837538	113837539	G	A	16	GENIC	homozygous	54228874
7	113841569	113841570	T	TAGC	3	GENIC	homozygous	54228876
7	113842425	113842426	C	CCATTTCAAGAGT	6	GENIC	homozygous	54067363
7	113845218	113845219	T	-	3	GENIC	homozygous	54228878
7	113845859	113845860	G	A	15	GENIC	possibly homozygous	54228880
7	113847218	113847219	A	-	2	GENIC	homozygous	54228882
7	113849674	113849675	C	T	6	GENIC	homozygous	54228884
7	113850620	113850621	A	G	27	GENIC	homozygous	54067373
7	113851006	113851007	G	T	26	GENIC	possibly homozygous	54228886
7	113853692	113853693	T	A	26	GENIC	homozygous	54228891
7	113857051	113857052	C	-	9	GENIC	heterozygous	54802201
7	113859287	113859288	G	GTTT	1	GENIC	homozygous	54228893
7	113860455	113860456	A	-	16	GENIC	homozygous	54067416
7	113861910	113861911	A	G	26	GENIC	homozygous	54228895
7	113862643	113862644	G	-	5	GENIC	homozygous	54067420
7	113863738	113863739	G	T	4	GENIC	homozygous	54228897
7	113863739	113863740	C	T	4	GENIC	homozygous	54228898
7	113868446	113868447	C	T	17	GENIC	possibly homozygous	54228900
7	113868953	113868954	A	C	7	GENIC	possibly homozygous	54067431
7	113869847	113869848	T	C	29	GENIC	possibly homozygous	54067432
7	113870275	113870276	T	G	21	GENIC	homozygous	54067434
7	113870950	113870951	A	T	14	GENIC	possibly homozygous	54067435
7	113871094	113871095	T	C	9	GENIC	homozygous	54067436
7	113872900	113872901	C	-	6	GENIC	heterozygous	54067438
7	113873692	113873693	A	G	3	GENIC	homozygous	54067439
7	113873773	113873774	C	CTT	4	GENIC	homozygous	54067440
7	113873804	113873805	G	A	5	GENIC	homozygous	54228908
7	113873816	113873817	A	C	6	GENIC	homozygous	54228910
7	113874102	113874103	A	C	31	GENIC	possibly homozygous	54228914