chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	10323987	10323988	A	C	28	GENIC	possibly homozygous	56745839
4	10324066	10324067	A	G	29	GENIC	heterozygous	56745840
4	10324454	10324460	AACAAC	------	8	GENIC	homozygous	56745841
4	10324970	10324971	T	C	78	GENIC	homozygous	56745842
4	10326302	10326303	T	C	46	GENIC	homozygous	56745843
4	10327411	10327433	TGTGTGTGTGTGTGTGTGTGTG	----------------------	2	GENIC	homozygous	56745844
4	10327454	10327455	T	G	20	GENIC	homozygous	56745845
4	10327456	10327457	A	G	19	GENIC	homozygous	56745846
4	10327464	10327465	A	G	28	GENIC	possibly homozygous	56745847
4	10327561	10327562	G	A	50	GENIC	homozygous	56745848
4	10327661	10327662	T	TCA	38	GENIC	homozygous	56745849
4	10327715	10327716	C	CA	46	GENIC	homozygous	56745850
4	10328426	10328429	TGT	---	6	GENIC	heterozygous	56745851
4	10328428	10328431	TGT	---	4	GENIC	homozygous	56745852
4	10328661	10328662	C	G	46	GENIC	homozygous	56745853
4	10329203	10329204	C	G	69	GENIC	homozygous	56745854