chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14273580	14273581	C	T	47	GENIC	homozygous	111452642
3	14273624	14273625	A	G	42	GENIC	homozygous	111452643
3	14274704	14274705	G	A	62	GENIC	homozygous	111452644
3	14275484	14275485	T	C	37	GENIC	homozygous	111452645
3	14276278	14276279	A	T	59	GENIC	homozygous	111452646
3	14276371	14276372	T	C	37	GENIC	homozygous	111452647
3	14277114	14277115	G	A	32	GENIC	possibly homozygous	111452648
3	14277551	14277552	T	C	38	GENIC	homozygous	111452649
3	14278498	14278498		AGAC	13	GENIC	homozygous	127851834
3	14276174	14276175	A		43	GENIC	homozygous	127851832
3	14278547	14278548	T	C	30	GENIC	homozygous	111452651
3	14279077	14279078	G	A	37	GENIC	homozygous	111452652
3	14280167	14280168	G	A	42	GENIC	homozygous	111452653
3	14281275	14281275		TGGGGATTTAGCTCAGTGGTAGAGCG	20	GENIC	homozygous	127851835
3	14281280	14281280		CTAGCAAGCA	29	GENIC	homozygous	127851836
3	14281869	14281870	C	T	38	GENIC	homozygous	111452654
3	14285943	14285944	G	A	38	GENIC	homozygous	111452655
3	14286937	14286937		TA	48	GENIC	homozygous	127851837
3	14287598	14287599	T	A	37	GENIC	homozygous	111452657
3	14281278	14281279	T	G	29	GENIC	homozygous	127968578
3	14286280	14286281	T	C	52	GENIC	homozygous	111452656
3	14287666	14287667	G		33	GENIC	homozygous	127851838