chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	144162539	144162539		CCT	35	GENIC	homozygous	128249721
5	144163972	144163973	C	T	46	GENIC	homozygous	114036704
5	144164471	144164472	T	A	34	GENIC	homozygous	114253947
5	144164535	144164535		CCAAGATG	32	GENIC	homozygous	128249722
5	144164589	144164590	C	T	42	GENIC	homozygous	114253949
5	144164594	144164595	T	G	41	GENIC	homozygous	114253951
5	144166417	144166418	G	T	66	GENIC	homozygous	114036705
5	144167500	144167501	C	G	44	GENIC	homozygous	114253953
5	144167565	144167566	T	C	52	GENIC	homozygous	114036706
5	144169769	144169770	A	T	34	GENIC	homozygous	114253955
5	144169921	144169922	T	C	65	GENIC	homozygous	114036707
5	144169938	144169939	A	G	66	GENIC	homozygous	114036708
5	144171171	144171172	A	G	54	GENIC	homozygous	114036709
5	144172133	144172134	G	A	56	GENIC	homozygous	114253957
5	144172935	144172936	C	T	46	GENIC	homozygous	114253959
5	144173916	144173917	C	T	56	GENIC	homozygous	114253961
5	144174710	144174711	T	C	23	GENIC	homozygous	114036711
5	144174847	144174847		T	41	GENIC	homozygous	128249725
5	144175239	144175240	G	T	49	GENIC	homozygous	114036712
5	144176574	144176575	C	A	45	GENIC	possibly homozygous	114152226
5	144176990	144176991	G	C	65	GENIC	homozygous	114152227