chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	90339585	90339586	G	T	28	GENIC	homozygous	114229578
5	90340374	90340375	T	A	14	GENIC	homozygous	114229579
5	90340898	90340899	A	C	32	GENIC	homozygous	113916062
5	90343733	90343734	G	T	34	GENIC	homozygous	113916068
5	90344508	90344509	A	G	30	GENIC	homozygous	113916071
5	90346408	90346409	T	A	25	GENIC	homozygous	113916074
5	90347494	90347495	T	C	37	GENIC	homozygous	114229583
5	90340966	90340967	T	A	20	GENIC	homozygous	114229580
5	90341493	90341494	G	A	26	GENIC	homozygous	114229581
5	90342068	90342069	C	T	32	GENIC	homozygous	114229582
5	90347803	90347804	A	C	36	GENIC	homozygous	113916077
5	90348334	90348335	A	C	18	GENIC	homozygous	113916081
5	90348503	90348504	C	T	29	GENIC	homozygous	113916082
5	90349682	90349683	A	G	24	GENIC	homozygous	114229584
5	90351303	90351304	T	C	28	GENIC	homozygous	113916089
5	90351393	90351394	A	G	19	GENIC	homozygous	113916090
5	90352041	90352042	T	C	23	GENIC	homozygous	113916094
5	90352053	90352054	C	T	25	GENIC	homozygous	114229585
5	90353165	90353166	C	T	38	GENIC	homozygous	114229586