chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	82590567	82590568	C	T	12	GENIC	homozygous	113896043
5	82592153	82592154	T	A	12	GENIC	homozygous	113896044
5	82593329	82593330	A	G	13	GENIC	homozygous	113896045
5	82593427	82593428	A	T	18	GENIC	homozygous	113896046
5	82593530	82593531	G	A	17	GENIC	homozygous	113896047
5	82593596	82593597	C	A	13	GENIC	homozygous	113896048
5	82593776	82593777	A	G	9	GENIC	homozygous	113896049
5	82594242	82594243	T	C	7	GENIC	homozygous	113896050
5	82594725	82594726	T	C	16	GENIC	homozygous	113896051
5	82594898	82594899	G	A	12	GENIC	homozygous	113896052
5	82595007	82595008	A	G	8	GENIC	homozygous	113896053
5	82595191	82595192	T	C	9	GENIC	homozygous	113896054
5	82595326	82595327	A	C	16	GENIC	homozygous	113896055
5	82596742	82596743	G	T	14	GENIC	homozygous	113896056
5	82596797	82596798	C	T	18	GENIC	homozygous	113896057
5	82596903	82596904	T	A	20	GENIC	heterozygous	114596427
5	82596945	82596946	T	C	14	GENIC	homozygous	113896058
5	82597068	82597069	T	C	5	GENIC	homozygous	113896059
5	82598159	82598160	C	T	16	GENIC	homozygous	113896060
5	82600548	82600549	T	G	14	GENIC	homozygous	113896061
5	82601030	82601031	A	T	27	GENIC	homozygous	113896062