chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208141687	208141688	T	TC	16	GENIC	homozygous	59357240
2	208142167	208142168	G	C	26	GENIC	homozygous	59357241
2	208142234	208142235	G	C	35	GENIC	homozygous	59357242
2	208142239	208142240	G	T	30	GENIC	homozygous	59771535
2	208142241	208142242	T	C	30	GENIC	homozygous	59771536
2	208142249	208142250	A	T	23	GENIC	homozygous	59357243
2	208142251	208142252	G	C	24	GENIC	homozygous	59357244
2	208142255	208142256	A	C	24	GENIC	homozygous	59357245
2	208142260	208142261	G	C	26	GENIC	homozygous	59357246
2	208142262	208142263	G	-	27	GENIC	homozygous	59357247
2	208143321	208143322	C	CTT	3	GENIC	heterozygous	60561357
2	208144252	208144253	G	GT	3	GENIC	heterozygous	60561358
2	208146439	208146440	G	A	30	GENIC	homozygous	60301260
2	208146698	208146699	T	C	35	GENIC	homozygous	59932033
2	208146959	208146960	G	T	29	GENIC	homozygous	60456715
2	208146960	208146961	T	C	28	GENIC	homozygous	60340599
2	208147008	208147009	T	C	35	GENIC	homozygous	60301261
2	208147342	208147343	G	A	39	GENIC	homozygous	60301262
2	208148019	208148020	A	G	23	GENIC	homozygous	60301263
2	208148882	208148883	T	TAA	2	GENIC	homozygous	60825916
2	208148929	208148930	A	AGG	4	GENIC	homozygous	60456716
2	208149036	208149037	A	G	7	GENIC	heterozygous	60456717
2	208149526	208149527	T	C	29	GENIC	homozygous	60301264
2	208150687	208150688	G	A	28	GENIC	homozygous	60301265