chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	106379769	106379770	C	A	24	GENIC	homozygous	113536211
14	106383139	106383140	C	T	22	GENIC	homozygous	113536213
14	106383713	106383714	C	T	15	GENIC	homozygous	113536215
14	106384747	106384748	C	T	22	GENIC	homozygous	113536217
14	106385278	106385279	T	A	22	GENIC	homozygous	113536221
14	106385389	106385390	C	T	17	GENIC	homozygous	113536223
14	106385720	106385721	T	C	17	GENIC	homozygous	113536225
14	106385768	106385769	A	C	21	GENIC	homozygous	113536227
14	106385816	106385817	C	T	30	GENIC	homozygous	113536229
14	106387051	106387052	T	C	23	GENIC	homozygous	113536231
14	106387124	106387125	T	C	17	GENIC	homozygous	113536233
14	106390744	106390745	G	A	14	GENIC	homozygous	113536235
14	106390931	106390932	C	T	29	GENIC	homozygous	113536237
14	106391980	106391981	T	C	18	GENIC	homozygous	113536239
14	106392713	106392714	A	G	22	GENIC	homozygous	113536241
14	106393116	106393117	C	T	28	GENIC	homozygous	113536243
14	106385056	106385057	T	C	10	GENIC	homozygous	114093323