chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	127506357	127506358	T	C	41	GENIC	homozygous	114001455
5	127507444	127507445	T	C	39	GENIC	homozygous	114001457
5	127507682	127507683	C	T	41	GENIC	homozygous	114001459
5	127508249	127508250	C	A	17	GENIC	homozygous	114001461
5	127508566	127508567	G	A	38	GENIC	homozygous	114001463
5	127508633	127508634	T	C	47	GENIC	homozygous	114001465
5	127508866	127508867	C	T	33	GENIC	homozygous	114001467
5	127508963	127508964	C	T	27	GENIC	homozygous	114001469
5	127509157	127509158	G	A	28	GENIC	homozygous	114001471
5	127509341	127509342	A	C	29	GENIC	homozygous	114001473
5	127509475	127509476	T	G	19	GENIC	homozygous	114001475
5	127509740	127509741	G	A	34	GENIC	homozygous	114001477
5	127510017	127510018	C	T	37	GENIC	homozygous	114001479
5	127511472	127511473	C	T	16	GENIC	homozygous	114001481
5	127512082	127512083	G	A	31	GENIC	homozygous	114001483
5	127512173	127512174	C	T	27	GENIC	homozygous	114529808
5	127512201	127512202	C	T	27	GENIC	homozygous	114001485
5	127512828	127512829	A	G	33	GENIC	homozygous	114001491
5	127512992	127512993	T	C	13	GENIC	homozygous	114001492
5	127515381	127515382	G	T	23	GENIC	homozygous	114001494
5	127519904	127519905	C	T	31	GENIC	homozygous	114529810
5	127520186	127520187	G	A	43	GENIC	homozygous	114001498