chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	64456232	64456233	C	T	25	GENIC	homozygous	47485250
16	64456387	64456388	A	C	34	GENIC	possibly homozygous	47818966
16	64456490	64456491	T	C	43	GENIC	homozygous	47818968
16	64456872	64456873	G	A	48	GENIC	possibly homozygous	47818970
16	64457265	64457266	A	G	45	GENIC	homozygous	47818972
16	64457309	64457310	C	T	40	GENIC	homozygous	47818974
16	64457631	64457634	GAG	---	23	GENIC	homozygous	47818976
16	64457872	64457873	C	CTAGCAGATATCT	2	GENIC	homozygous	47485251
16	64458704	64458705	T	C	37	GENIC	homozygous	47485252
16	64458851	64458852	G	T	38	GENIC	homozygous	47485253
16	64459207	64459208	G	A	44	GENIC	homozygous	47485254
16	64459362	64459363	T	C	31	GENIC	possibly homozygous	47485255
16	64459462	64459463	A	G	33	GENIC	homozygous	47485256
16	64459581	64459582	C	A	17	GENIC	homozygous	47818978
16	64459605	64459617	ATATGTGTGTGT	------------	8	GENIC	heterozygous	47485257
16	64457569	64457570	A	G	23	GENIC	possibly homozygous	47684844
16	64459641	64459642	G	GCA	12	GENIC	heterozygous	47768336
16	64459650	64459651	C	CACACACGCGCGCGT	21	GENIC	homozygous	47768337
16	64459919	64459920	C	T	26	GENIC	homozygous	47818980
16	64460054	64460056	AC	--	40	GENIC	homozygous	47485258
16	64460055	64460056	C	-	42	GENIC	homozygous	47485259
16	64460084	64460085	C	-	37	GENIC	possibly homozygous	47684858
16	64460225	64460226	G	T	44	GENIC	homozygous	47485261
16	64460305	64460306	C	T	39	GENIC	homozygous	47485262
16	64460362	64460363	A	C	41	GENIC	homozygous	47818982
16	64461845	64461846	T	C	35	GENIC	homozygous	47485264