chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135446592	135446593	A	C	58	GENIC	homozygous	114144467
5	135446596	135446598	AT		59	GENIC	homozygous	128242411
5	135446919	135446920	G	A	83	GENIC	homozygous	114144468
5	135449328	135449329	T	C	48	GENIC	homozygous	114017987
5	135451481	135451482	C	A	74	GENIC	homozygous	114144469
5	135455276	135455277	C	T	63	GENIC	homozygous	114017993
5	135455412	135455413	C	T	58	GENIC	homozygous	114144471
5	135456626	135456627	C	T	52	GENIC	homozygous	114144472
5	135456857	135456858	C	A	72	GENIC	homozygous	114017994
5	135457522	135457522		A	40	GENIC	homozygous	128242413
5	135457612	135457614	AA		49	GENIC	homozygous	128242414
5	135457685	135457686	A	G	50	GENIC	homozygous	114144473
5	135459902	135459903	G	A	14	GENIC	possibly homozygous	114144474
5	135460026	135460027	C	A	47	GENIC	homozygous	114144475
5	135460742	135460743	C	A	48	GENIC	homozygous	114144476
5	135460850	135460851	C	T	60	GENIC	homozygous	114017995
5	135461914	135461915	C	T	46	GENIC	homozygous	114144477
5	135462114	135462114		C	46	GENIC	homozygous	131650117
5	135462119	135462119		C	50	GENIC	homozygous	131650118
5	135463891	135463892	G	A	76	GENIC	homozygous	114017998
5	135465749	135465752	GTT		29	GENIC	homozygous	131650119
5	135468210	135468211	G	A	46	GENIC	homozygous	114144478
5	135469241	135469242	A	G	50	GENIC	homozygous	114144479
5	135469795	135469796	A	G	51	GENIC	possibly homozygous	114018003
5	135469795	135469795		G	49	GENIC	possibly homozygous	131650120
5	135471437	135471438	A	G	54	GENIC	homozygous	114018005
5	135457000	135457001	A	G	52	GENIC	homozygous	114442364