chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59244730	59244750	ACTGCCTTCAGTGGTCTCTT		52	GENIC	homozygous	137310909
5	59244754	59244757	CCA		51	GENIC	homozygous	137310910
5	59248648	59248649	T	G	53	GENIC	homozygous	137479431
5	59249783	59249784	A	G	47	GENIC	homozygous	137479432
5	59250425	59250426	G		24	GENIC	homozygous	137310911
5	59250457	59250458	A	G	13	GENIC	heterozygous	147795636
5	59250637	59250638	C	T	58	GENIC	homozygous	137479433
5	59250921	59250922	A	T	49	GENIC	homozygous	137479434
5	59251578	59251579	C	T	48	GENIC	homozygous	137479435
5	59254805	59254806	A	G	50	GENIC	homozygous	137479436
5	59255454	59255455	C	A	50	GENIC	possibly homozygous	137479437
5	59256039	59256040	A		40	GENIC	homozygous	137310912
5	59257705	59257706	A	G	37	GENIC	homozygous	137479438
5	59257880	59257881	T	A	51	GENIC	possibly homozygous	137479439
5	59258271	59258271		A	33	GENIC	possibly homozygous	137310913
5	59258280	59258281	T	A	39	GENIC	possibly homozygous	137479440
5	59258372	59258372		G	15	GENIC	homozygous	137310914
5	59258565	59258566	T	A	46	GENIC	homozygous	137479441
5	59260794	59260795	A	T	62	GENIC	homozygous	137479442
5	59261193	59261194	C	G	52	GENIC	homozygous	137479443
5	59261451	59261452	A	G	53	GENIC	homozygous	137479444
5	59261805	59261806	C	T	54	GENIC	homozygous	137479445
5	59261852	59261853	C	A	56	GENIC	homozygous	137479446
5	59261972	59261973	A	G	52	GENIC	homozygous	137479447
5	59262220	59262220		T	47	GENIC	possibly homozygous	137310915
5	59262824	59262825	C		65	GENIC	homozygous	137310916
5	59262854	59262855	T	C	70	GENIC	homozygous	137479448
5	59263236	59263237	C	T	53	GENIC	homozygous	137479449
5	59263412	59263417	GGACA		41	GENIC	homozygous	137310917
5	59265432	59265433	T	C	27	GENIC	homozygous	137479450