chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	236049567	236049568	T		40	GENIC	homozygous	142796938
1	236049572	236049578	CCCCCA		40	GENIC	homozygous	142796939
1	236049577	236049578	A		40	GENIC	homozygous	402981978
1	236049577	236049578	A	C	40	GENIC	heterozygous	402981979
1	236061234	236061235	G	A	58	GENIC	possibly homozygous	142874986
1	236049777	236049778	T	A	58	GENIC	homozygous	142874983
1	236053710	236053711	C	T	28	GENIC	homozygous	142874984
1	236059891	236059892	C	G	58	GENIC	homozygous	142874985
1	236063668	236063669	T	C	48	GENIC	homozygous	135838894
1	236065388	236065389	G	A	55	GENIC	homozygous	142874987
1	236066290	236066291	G	A	43	GENIC	homozygous	142874988
1	236067381	236067381		A	44	GENIC	homozygous	142796940
1	236068443	236068443		C	42	GENIC	homozygous	142796941
1	236068918	236068918		T	27	GENIC	possibly homozygous	135467036
1	236077873	236077874	T	A	47	GENIC	homozygous	135838904
1	236082633	236082637	AAAG		56	GENIC	homozygous	142796943
1	236078107	236078108	A	G	24	GENIC	heterozygous	403762304
1	236078107	236078108	A		24	GENIC	homozygous	403762303