chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150959744	150959745	G	T	54	GENIC	possibly homozygous	137651472
5	150959767	150959768	G	A	51	GENIC	homozygous	137651473
5	150961840	150961841	T	C	50	GENIC	homozygous	137651474
5	150962466	150962467	G	A	35	GENIC	homozygous	137651475
5	150962584	150962585	A	C	39	GENIC	homozygous	137651476
5	150962662	150962663	A	G	34	GENIC	homozygous	137651477
5	150963348	150963349	G	A	40	GENIC	homozygous	137651478
5	150964169	150964170	C	T	47	GENIC	homozygous	137651479
5	150965231	150965232	G	A	43	GENIC	homozygous	137651480
5	150965327	150965328	G	A	35	GENIC	homozygous	137651481
5	150967061	150967062	T	C	37	GENIC	homozygous	137651482
5	150967277	150967278	A	G	39	GENIC	homozygous	137651483
5	150967852	150967853	C	T	28	GENIC	homozygous	137651484
5	150969291	150969292	G	A	36	GENIC	homozygous	137651485
5	150970451	150970452	G	A	45	GENIC	homozygous	137651486
5	150971310	150971311	A	G	52	GENIC	homozygous	137651487
5	150972880	150972881	G	A	43	GENIC	homozygous	137651488
5	150975457	150975458	G	A	22	GENIC	homozygous	137651489
5	150976880	150976881	T	A	52	GENIC	homozygous	137651490
5	150967847	150967847		AC	30	GENIC	homozygous	137349152
5	150969370	150969370		TGCCACCACG	32	GENIC	possibly homozygous	137349153
5	150980395	150980396	G	A	42	GENIC	homozygous	137651491
5	150980944	150980945	G	A	43	GENIC	homozygous	137651492
5	150981054	150981055	C	A	42	GENIC	homozygous	137651493
5	150981120	150981121	A		33	GENIC	homozygous	137349154
5	150981177	150981178	A	G	15	GENIC	homozygous	137651494