chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	80194324	80194325	T	C	44	GENIC	homozygous	113500490
14	80195231	80195232	G	A	28	GENIC	possibly homozygous	118703580
14	80197083	80197084	C	G	44	GENIC	homozygous	113500492
14	80197777	80197778	T	C	56	GENIC	homozygous	113500494
14	80197827	80197828	A	G	52	GENIC	possibly homozygous	113500496
14	80197978	80197979	A	G	30	GENIC	homozygous	113500498
14	80199263	80199264	A	G	43	GENIC	homozygous	113500500
14	80200129	80200130	C	T	52	GENIC	homozygous	113500502
14	80212523	80212524	C	A	63	GENIC	homozygous	113500504
14	80212881	80212882	C	A	62	GENIC	homozygous	113500506
14	80213871	80213872	C	T	53	GENIC	homozygous	113500508
14	80213952	80213953	G	A	38	GENIC	homozygous	113500510
14	80214045	80214046	C	T	28	GENIC	homozygous	113500512
14	80214128	80214129	G	A	39	GENIC	homozygous	113500514
14	80214279	80214280	T	A	48	GENIC	homozygous	113500516
14	80214589	80214590	A	G	67	GENIC	homozygous	113500518
14	80214605	80214606	C	A	70	GENIC	homozygous	113500520
14	80214679	80214680	G	T	57	GENIC	homozygous	113500522
14	80215583	80215584	T	A	52	GENIC	homozygous	113500524
14	80217095	80217096	G	C	128	GENIC	heterozygous	118703581
14	80217103	80217104	A	G	148	GENIC	heterozygous	118703582
14	80217157	80217158	G	A	118	GENIC	heterozygous	118703583
14	80217362	80217363	A	G	70	GENIC	homozygous	113500525
14	80218967	80218968	G	A	47	GENIC	possibly homozygous	113500526
14	80220004	80220005	T	C	42	GENIC	homozygous	113500527
14	80221630	80221631	A	G	25	GENIC	homozygous	113500528
14	80223311	80223312	A	G	49	GENIC	homozygous	113500529
14	80223497	80223498	A	G	44	GENIC	homozygous	113500530
14	80227184	80227185	G	C	51	GENIC	homozygous	113500531
14	80228084	80228085	G	T	59	GENIC	possibly homozygous	113500532
14	80228752	80228753	A	C	43	GENIC	homozygous	113500534
14	80216436	80216437	G	A	29	GENIC	homozygous	114222804
14	80212103	80212104	C	G	24	GENIC	homozygous	114026059
14	80216435	80216436	T	C	29	GENIC	possibly homozygous	114222802