chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	144161887	144161888	C	T	11	GENIC	homozygous	114036701
5	144162539	144162539		CCT	16	GENIC	homozygous	128249721
5	144163041	144163042	C	T	18	GENIC	homozygous	114036702
5	144163151	144163152	C	A	26	GENIC	homozygous	114036703
5	144163972	144163973	C	T	17	GENIC	homozygous	114036704
5	144164535	144164535		CCAAGATG	10	GENIC	homozygous	128249722
5	144166417	144166418	G	T	30	GENIC	homozygous	114036705
5	144167565	144167566	T	C	19	GENIC	homozygous	114036706
5	144169921	144169922	T	C	24	GENIC	homozygous	114036707
5	144169938	144169939	A	G	25	GENIC	homozygous	114036708
5	144170280	144170281	C		12	GENIC	homozygous	128249723
5	144171171	144171172	A	G	22	GENIC	homozygous	114036709
5	144171210	144171211	G	C	24	GENIC	homozygous	114036710
5	144173685	144173686	C	A	35	GENIC	homozygous	118846232
5	144174150	144174150		A	20	GENIC	homozygous	128249724
5	144174710	144174711	T	C	9	GENIC	homozygous	114036711
5	144174847	144174847		T	22	GENIC	possibly homozygous	128249725
5	144175239	144175240	G	T	12	GENIC	homozygous	114036712
5	144175369	144175370	G	A	16	GENIC	homozygous	114036713
5	144175453	144175454	C	T	18	GENIC	homozygous	114036714
5	144177340	144177341	A	G	12	GENIC	homozygous	114036715
5	144177820	144177821	A	G	13	GENIC	homozygous	114036716