chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14273624	14273625	A	G	18	GENIC	homozygous	111452643
3	14274662	14274663	C	T	23	GENIC	homozygous	112406844
3	14274856	14274857	A	G	32	GENIC	homozygous	112406846
3	14275259	14275260	A	T	25	GENIC	homozygous	111879474
3	14275484	14275485	T	C	21	GENIC	homozygous	111452645
3	14275802	14275803	G	A	28	GENIC	homozygous	112406848
3	14276278	14276279	A	T	36	GENIC	homozygous	111452646
3	14276371	14276372	T	C	25	GENIC	homozygous	111452647
3	14277114	14277115	G	A	20	GENIC	homozygous	111452648
3	14277483	14277484	G	T	27	GENIC	homozygous	120038505
3	14277602	14277603	C	T	29	GENIC	homozygous	111879480
3	14275980	14275981	G		11	GENIC	homozygous	135034084
3	14275986	14275992	CCCCTT		12	GENIC	homozygous	135034085
3	14275993	14275996	GTC		12	GENIC	homozygous	135034086
3	14278547	14278548	T	C	23	GENIC	homozygous	111452651
3	14278675	14278676	G	A	33	GENIC	homozygous	112406850
3	14281275	14281275		TGGGGATTTAGCTCAGTGGTAGAGCG	4	GENIC	homozygous	127851835
3	14281278	14281279	T	G	6	GENIC	homozygous	127968578
3	14281280	14281280		CTAGCAAGCA	6	GENIC	homozygous	127851836
3	14281324	14281324		A	14	GENIC	possibly homozygous	135034087
3	14286937	14286937		TA	14	GENIC	homozygous	127851837
3	14287598	14287599	T	A	29	GENIC	homozygous	111452657
3	14282205	14282206	C	T	21	GENIC	possibly homozygous	112406852
3	14284899	14284900	A	C	23	GENIC	homozygous	112406854
3	14286280	14286281	T	C	22	GENIC	homozygous	111452656
3	14287666	14287667	G		29	GENIC	homozygous	127851838
3	14290847	14290854	AAAAAAC		19	GENIC	possibly homozygous	132038805