chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	144162299	144162300	T	C	12	GENIC	homozygous	126329089
5	144163972	144163973	C	T	18	GENIC	homozygous	114036704
5	144164535	144164535		CCAAGATG	10	GENIC	homozygous	128249722
5	144165566	144165567	A	T	26	GENIC	homozygous	122409207
5	144166417	144166418	G	T	20	GENIC	homozygous	114036705
5	144167565	144167566	T	C	19	GENIC	homozygous	114036706
5	144168090	144168091	C	A	12	GENIC	homozygous	126329091
5	144169921	144169922	T	C	22	GENIC	homozygous	114036707
5	144169938	144169939	A	G	23	GENIC	homozygous	114036708
5	144171171	144171172	A	G	23	GENIC	homozygous	114036709
5	144171813	144171814	T	C	26	GENIC	homozygous	126329093
5	144164035	144164035		TG	14	GENIC	possibly homozygous	130315135
5	144173258	144173259	A	C	20	GENIC	homozygous	126329095
5	144174710	144174711	T	C	4	GENIC	homozygous	114036711
5	144175239	144175240	G	T	21	GENIC	homozygous	114036712
5	144177820	144177821	A	G	17	GENIC	homozygous	114036716
5	144172719	144172721	TA		10	GENIC	homozygous	135313021
5	144170002	144170002		C	21	GENIC	homozygous	135313019
5	144170876	144170885	AACTGATGA		19	GENIC	possibly homozygous	135313020
5	144175453	144175454	C	T	23	GENIC	homozygous	114036714
5	144177198	144177199	C	T	22	GENIC	homozygous	126329097
5	144177340	144177341	A	G	23	GENIC	homozygous	114036715
5	144172817	144172818	G	A	8	GENIC	homozygous	135318279