chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	214696690	214696691	T	TAA	11	GENIC	heterozygous	57081080
4	214698797	214698800	AAA	---	13	GENIC	homozygous	58371837
4	214698799	214698800	A	ATT	12	GENIC	homozygous	58371839
4	214698993	214698995	AC	--	5	GENIC	homozygous	58371841
4	214701530	214701531	C	T	20	GENIC	homozygous	57081082
4	214701658	214701659	C	T	25	GENIC	homozygous	57081083
4	214701781	214701782	C	A	15	GENIC	homozygous	57081084
4	214702040	214702041	C	T	13	GENIC	possibly homozygous	57081085
4	214702048	214702049	A	T	13	GENIC	possibly homozygous	57081086
4	214702055	214702056	A	G	13	GENIC	possibly homozygous	57081087
4	214702059	214702060	C	T	15	GENIC	heterozygous	57081088
4	214702142	214702143	G	A	22	GENIC	possibly homozygous	57081089
4	214702388	214702389	T	C	20	GENIC	homozygous	57081090
4	214702438	214702439	T	C	20	GENIC	homozygous	57081091
4	214702442	214702443	T	A	19	GENIC	homozygous	57081092
4	214702448	214702449	A	G	21	GENIC	homozygous	57081093
4	214702531	214702532	T	TAGGCATGTCTGC	18	GENIC	homozygous	57081095
4	214702654	214702655	T	C	14	GENIC	homozygous	57081096
4	214702796	214702797	T	-	26	GENIC	homozygous	57081097
4	214702982	214702983	T	C	27	GENIC	homozygous	57081098