chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	106379769	106379770	C	A	17	GENIC	homozygous	113536211
14	106383139	106383140	C	T	43	GENIC	homozygous	113536213
14	106383713	106383714	C	T	43	GENIC	homozygous	113536215
14	106384747	106384748	C	T	14	GENIC	homozygous	113536217
14	106385058	106385059	G	A	16	GENIC	homozygous	113536219
14	106385278	106385279	T	A	26	GENIC	homozygous	113536221
14	106385389	106385390	C	T	20	GENIC	possibly homozygous	113536223
14	106385720	106385721	T	C	41	GENIC	homozygous	113536225
14	106385768	106385769	A	C	43	GENIC	homozygous	113536227
14	106385816	106385817	C	T	27	GENIC	homozygous	113536229
14	106387051	106387052	T	C	48	GENIC	homozygous	113536231
14	106387124	106387125	T	C	40	GENIC	homozygous	113536233
14	106390744	106390745	G	A	61	GENIC	homozygous	113536235
14	106390931	106390932	C	T	36	GENIC	homozygous	113536237
14	106391980	106391981	T	C	55	GENIC	homozygous	113536239
14	106392713	106392714	A	G	13	GENIC	homozygous	113536241
14	106393116	106393117	C	T	32	GENIC	homozygous	113536243