chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	14679694	14679695	A	G	61	GENIC	homozygous	137384694
5	14679935	14679936	C	T	58	GENIC	homozygous	137384695
5	14684690	14684691	T	C	48	GENIC	homozygous	137384696
5	14685039	14685040	T	C	46	GENIC	homozygous	137384697
5	14685790	14685791	G	A	42	GENIC	homozygous	137384698
5	14690792	14690793	A	C	63	GENIC	homozygous	137384699
5	14691784	14691785	A	G	53	GENIC	homozygous	137384700
5	14694404	14694405	C	T	50	GENIC	homozygous	137384701
5	14696886	14696887	C	G	39	GENIC	homozygous	137384702
5	14703357	14703358	A	C	47	GENIC	homozygous	137384703
5	14706689	14706690	T	A	39	GENIC	homozygous	137384704
5	14707537	14707538	T	C	59	GENIC	homozygous	137384705
5	14699333	14699334	A		28	GENIC	heterozygous	403891982
5	14692168	14692168		ACAC	50	GENIC	homozygous	137291855
5	14699333	14699334	A	T	28	GENIC	possibly homozygous	154264964
5	14706098	14706099	A	G	29	GENIC	heterozygous	154264966
5	14706104	14706105	A	G	29	GENIC	possibly homozygous	154264967
5	14706102	14706103	A		29	GENIC	possibly homozygous	403891983
5	14706102	14706103	A	G	29	GENIC	heterozygous	403891984
5	14706098	14706099	A		29	GENIC	possibly homozygous	403592750
5	14706100	14706101	A		29	GENIC	possibly homozygous	403592751
5	14706100	14706101	A	G	29	GENIC	heterozygous	403592752
5	14706104	14706105	A		29	GENIC	heterozygous	403993640
5	14706106	14706107	A	G	31	GENIC	heterozygous	146774420