chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	142689059	142689060	C	T	14	GENIC	heterozygous	114033890
5	142689616	142689617	A	G	49	GENIC	homozygous	114033891
5	142689912	142689913	C	T	36	GENIC	homozygous	114033892
5	142690107	142690108	G	T	46	GENIC	homozygous	114033893
5	142690338	142690339	C	T	35	GENIC	homozygous	114033894
5	142690714	142690715	A	G	52	GENIC	homozygous	114033895
5	142690719	142690720	C	T	54	GENIC	homozygous	114033896
5	142690903	142690904	C	T	57	GENIC	homozygous	114033897
5	142691300	142691301	A	C	15	GENIC	homozygous	114033898
5	142692042	142692043	A	C	29	GENIC	homozygous	114033899
5	142692060	142692061	G	T	27	GENIC	possibly homozygous	114033900
5	142692740	142692741	T	C	68	GENIC	homozygous	114033901
5	142692964	142692965	A	G	57	GENIC	homozygous	114033902
5	142693280	142693281	G	A	46	GENIC	homozygous	114033903
5	142693686	142693687	C	T	32	GENIC	homozygous	114033904
5	142694796	142694797	C	T	49	GENIC	homozygous	114033905
5	142695469	142695470	G	A	41	GENIC	homozygous	114033906
5	142695901	142695902	T	C	35	GENIC	homozygous	114033907
5	142696239	142696240	T	C	44	GENIC	homozygous	114033908