chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	146737149	146737149		A	36	GENIC	possibly homozygous	143187414
5	146737300	146737301	A	G	47	GENIC	homozygous	143260745
5	146738473	146738474	A	T	23	GENIC	homozygous	146787217
5	146738718	146738718		T	40	GENIC	homozygous	143187415
5	146738770	146738771	G	A	36	GENIC	homozygous	143260746
5	146739187	146739188	G	C	53	GENIC	homozygous	143260747
5	146740120	146740120		TG	56	GENIC	homozygous	143187416
5	146741004	146741005	C	T	41	GENIC	homozygous	143260748
5	146741157	146741158	A	C	45	GENIC	homozygous	143260749
5	146741498	146741499	C	A	21	GENIC	homozygous	143260750
5	146741531	146741533	AG		11	GENIC	homozygous	143187417
5	146742405	146742406	T	G	56	GENIC	homozygous	143260751
5	146742534	146742535	C	T	38	GENIC	homozygous	143260752
5	146742840	146742841	A	G	53	GENIC	homozygous	143260753
5	146744265	146744266	A	C	49	GENIC	homozygous	143260754
5	146744414	146744415	A	C	54	GENIC	homozygous	143260755
5	146745329	146745330	G	A	62	GENIC	homozygous	143260756
5	146745556	146745557	G	C	46	GENIC	homozygous	143260757
5	146746214	146746215	A	G	62	GENIC	homozygous	143260758
5	146741532	146741533	G		11	GENIC	homozygous	403996199
5	146741532	146741533	G	C	11	GENIC	heterozygous	154257573