chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	104347687	104347688	C	A	16	GENIC	possibly homozygous	113529807
14	104348357	104348358	C	T	24	GENIC	homozygous	113529809
14	104349167	104349168	T	C	22	GENIC	homozygous	113529811
14	104349320	104349321	T	C	28	GENIC	homozygous	113529813
14	104349489	104349490	A	G	16	GENIC	homozygous	113529815
14	104349707	104349708	C	G	11	GENIC	homozygous	113529817
14	104350007	104350008	A	T	15	GENIC	homozygous	113529819
14	104351930	104351931	G	T	24	GENIC	homozygous	113529821
14	104352444	104352445	C	T	16	GENIC	homozygous	113529823
14	104352782	104352783	C	T	23	GENIC	homozygous	113529825
14	104353275	104353276	C	T	22	GENIC	homozygous	113529827
14	104354450	104354451	C	T	6	GENIC	homozygous	113615431
14	104354474	104354475	C	A	3	GENIC	homozygous	113764669
14	104357101	104357102	A	T	37	GENIC	homozygous	113615432
14	104357913	104357914	T	C	29	GENIC	homozygous	113529829
14	104358075	104358076	A	G	22	GENIC	homozygous	113529831
14	104360081	104360082	A	G	28	GENIC	homozygous	113529833
14	104360210	104360211	C	A	21	GENIC	homozygous	113529835
14	104360749	104360750	A	T	23	GENIC	homozygous	113529837
14	104360858	104360859	A	G	38	GENIC	homozygous	113529839
14	104365472	104365473	A	G	31	GENIC	homozygous	113529845
14	104366698	104366699	T	C	25	GENIC	homozygous	113529847
14	104370018	104370019	C	A	11	GENIC	homozygous	113529849
14	104370319	104370320	T	C	27	GENIC	homozygous	113529851
14	104371398	104371399	C	T	33	GENIC	homozygous	113529857
14	104371695	104371696	C	G	29	GENIC	homozygous	113529859
14	104371861	104371862	C	G	33	GENIC	homozygous	113529861
14	104371900	104371901	C	T	27	GENIC	homozygous	113529863
14	104373704	104373705	A	T	7	GENIC	homozygous	113615433