chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	104340252	104340253	C	T	31	GENIC	homozygous	113615429
14	104341358	104341359	T	C	26	GENIC	homozygous	113615430
14	104349167	104349168	T	C	43	GENIC	homozygous	113529811
14	104346650	104346651	A	G	24	GENIC	homozygous	113529805
14	104347687	104347688	C	A	26	GENIC	homozygous	113529807
14	104348357	104348358	C	T	29	GENIC	homozygous	113529809
14	104349320	104349321	T	C	33	GENIC	homozygous	113529813
14	104349489	104349490	A	G	22	GENIC	homozygous	113529815
14	104349707	104349708	C	G	18	GENIC	homozygous	113529817
14	104350007	104350008	A	T	25	GENIC	homozygous	113529819
14	104351930	104351931	G	T	30	GENIC	homozygous	113529821
14	104352444	104352445	C	T	27	GENIC	homozygous	113529823
14	104352782	104352783	C	T	27	GENIC	homozygous	113529825
14	104353275	104353276	C	T	29	GENIC	homozygous	113529827
14	104357913	104357914	T	C	28	GENIC	homozygous	113529829
14	104358075	104358076	A	G	29	GENIC	homozygous	113529831
14	104360081	104360082	A	G	18	GENIC	homozygous	113529833
14	104360210	104360211	C	A	21	GENIC	homozygous	113529835
14	104360749	104360750	A	T	20	GENIC	homozygous	113529837
14	104360858	104360859	A	G	25	GENIC	homozygous	113529839
14	104363996	104363997	C	A	16	GENIC	homozygous	113529841
14	104364572	104364573	G	A	23	GENIC	homozygous	113529843
14	104365472	104365473	A	G	44	GENIC	homozygous	113529845
14	104366698	104366699	T	C	32	GENIC	homozygous	113529847
14	104370018	104370019	C	A	16	GENIC	homozygous	113529849
14	104370319	104370320	T	C	29	GENIC	homozygous	113529851
14	104371398	104371399	C	T	42	GENIC	homozygous	113529857
14	104371695	104371696	C	G	33	GENIC	homozygous	113529859
14	104371861	104371862	C	G	37	GENIC	homozygous	113529861
14	104371900	104371901	C	T	32	GENIC	homozygous	113529863
14	104375823	104375824	T	C	5	GENIC	homozygous	113529865
14	104368171	104368172	T	G	6	GENIC	homozygous	114006249