chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	16413640	16413641	T	C	20	GENIC	homozygous	114177240
5	16415358	16415359	A	T	39	GENIC	homozygous	114177241
5	16416373	16416374	T	C	35	GENIC	homozygous	114177242
5	16416987	16416988	G	A	17	GENIC	homozygous	114177243
5	16418066	16418067	A	G	25	GENIC	homozygous	114177244
5	16418250	16418251	G	A	28	GENIC	homozygous	114177245
5	16422539	16422540	C	A	28	GENIC	homozygous	113673522
5	16422545	16422546	G	A	27	GENIC	homozygous	114177246
5	16422194	16422195	A	C	4	GENIC	heterozygous	119085727
5	16422196	16422197	A	C	4	GENIC	heterozygous	119085728
5	16423952	16423953	G	T	25	GENIC	possibly homozygous	114177247
5	16424393	16424394	C	A	24	GENIC	homozygous	114177248
5	16424686	16424687	A	C	26	GENIC	homozygous	113673524
5	16426833	16426834	T	G	9	GENIC	heterozygous	113673532
5	16428435	16428436	A	G	26	GENIC	homozygous	113673536
5	16429870	16429871	A	G	22	GENIC	homozygous	114177250
5	16431386	16431387	G	T	29	GENIC	possibly homozygous	114177251
5	16433034	16433035	G	A	21	GENIC	homozygous	114177252
5	16434248	16434249	T	C	32	GENIC	homozygous	114177253
5	16441279	16441280	C	T	29	GENIC	homozygous	114177259
5	16443161	16443162	A	C	28	GENIC	homozygous	114177260
5	16445094	16445095	A	C	38	GENIC	homozygous	113673594