chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	76402870	76402871	G	A	45	GENIC	homozygous	139346960
13	76402966	76402967	A	G	62	GENIC	homozygous	139346961
13	76402996	76402997	C	T	60	GENIC	homozygous	139346962
13	76403074	76403075	A	G	57	GENIC	homozygous	139346963
13	76403235	76403236	C	G	48	GENIC	homozygous	139346964
13	76403340	76403341	G	C	66	GENIC	homozygous	139346965
13	76403881	76403882	A	G	53	GENIC	homozygous	139346966
13	76404404	76404405	T	C	39	GENIC	homozygous	139346967
13	76404436	76404437	A	T	45	GENIC	homozygous	139346968
13	76404465	76404466	C	T	51	GENIC	homozygous	139346969
13	76404674	76404675	G		58	GENIC	homozygous	139185025
13	76404889	76404889		C	54	GENIC	homozygous	139185026
13	76405374	76405375	C	T	66	GENIC	homozygous	139346970
13	76405382	76405383	G	A	68	GENIC	homozygous	139346971
13	76405505	76405506	T	C	68	GENIC	homozygous	139346972
13	76405676	76405691	TGTTTGGCTCTCCCA		45	GENIC	homozygous	139185027
13	76406193	76406194	T	C	58	GENIC	homozygous	139346973
13	76406377	76406378	A	G	55	GENIC	homozygous	139346974
13	76406471	76406472	C	T	60	GENIC	homozygous	139346975
13	76408102	76408102		TG	26	GENIC	homozygous	139185028
13	76408495	76408496	C	T	53	GENIC	homozygous	139346976
13	76408808	76408809	A	G	59	GENIC	homozygous	139346977