chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	131837546	131837547	G	A	49	GENIC	homozygous	114141757
5	131844777	131844778	G	A	52	GENIC	homozygous	114009087
5	131845402	131845403	C	T	57	GENIC	homozygous	114009088
5	131845727	131845728	C	A	46	GENIC	homozygous	114009089
5	131846180	131846181	T	G	45	GENIC	homozygous	114009090
5	131847859	131847860	G	A	43	GENIC	homozygous	114141758
5	131848908	131848909	T	G	52	GENIC	homozygous	114009091
5	131849903	131849904	G	A	30	GENIC	homozygous	114141759
5	131849919	131849919		T	30	GENIC	homozygous	128239641
5	131849926	131849928	GA		37	GENIC	homozygous	128239642
5	131849944	131849944		T	38	GENIC	homozygous	128239643
5	131849991	131849992	A		39	GENIC	homozygous	128239644
5	131850010	131850011	C		36	GENIC	homozygous	128239645
5	131850051	131850051		C	28	GENIC	homozygous	128239646
5	131850089	131850090	A	T	25	GENIC	homozygous	114009101
5	131850142	131850143	C		36	GENIC	homozygous	128239647
5	131850151	131850152	A		36	GENIC	homozygous	128239648
5	131850180	131850181	A		38	GENIC	homozygous	128239649
5	131850195	131850196	C		38	GENIC	homozygous	128239650
5	131850202	131850202		C	38	GENIC	homozygous	128239651
5	131853410	131853411	A	G	51	GENIC	homozygous	114009103
5	131853511	131853512	T	G	53	GENIC	homozygous	114009104
5	131853678	131853679	T	C	50	GENIC	homozygous	114009105
5	131859483	131859484	T	C	50	GENIC	homozygous	114009108
5	131859936	131859937	G	A	53	GENIC	homozygous	114009109
5	131862290	131862291	C	G	59	GENIC	homozygous	114009111