chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	127506357	127506358	T	C	38	GENIC	homozygous	114001455
5	127507444	127507445	T	C	65	GENIC	homozygous	114001457
5	127507682	127507683	C	T	61	GENIC	homozygous	114001459
5	127508249	127508250	C	A	45	GENIC	homozygous	114001461
5	127508566	127508567	G	A	51	GENIC	homozygous	114001463
5	127508633	127508634	T	C	47	GENIC	homozygous	114001465
5	127508866	127508867	C	T	44	GENIC	homozygous	114001467
5	127508963	127508964	C	T	32	GENIC	homozygous	114001469
5	127509157	127509158	G	A	35	GENIC	homozygous	114001471
5	127509341	127509342	A	C	29	GENIC	homozygous	114001473
5	127509475	127509476	T	G	20	GENIC	homozygous	114001475
5	127509740	127509741	G	A	23	GENIC	homozygous	114001477
5	127510017	127510018	C	T	64	GENIC	homozygous	114001479
5	127511472	127511473	C	T	42	GENIC	homozygous	114001481
5	127512082	127512083	G	A	44	GENIC	homozygous	114001483
5	127512482	127512483	G	C	20	GENIC	homozygous	114001487
5	127512828	127512829	A	G	53	GENIC	homozygous	114001491
5	127515381	127515382	G	T	39	GENIC	homozygous	114001494
5	127517657	127517658	T	C	15	GENIC	homozygous	114001496
5	127520186	127520187	G	A	43	GENIC	homozygous	114001498