chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	59759032	59759033	C	G	23	GENIC	homozygous	108116355
1	59759423	59759424	G	A	29	GENIC	homozygous	108116356
1	59759560	59759561	T	C	22	GENIC	homozygous	108116357
1	59759748	59759749	T	C	31	GENIC	homozygous	108116358
1	59760068	59760069	A	G	18	GENIC	homozygous	108116359
1	59760170	59760171	A	G	26	GENIC	homozygous	108116360
1	59760188	59760189	T	C	26	GENIC	homozygous	108116361
1	59760266	59760267	C	T	24	GENIC	homozygous	108116362
1	59760397	59760398	G	A	22	GENIC	homozygous	108116363
1	59760781	59760782	A	G	34	GENIC	homozygous	108116364
1	59761975	59761976	A	T	28	GENIC	homozygous	108116373
1	59762427	59762428	C	G	27	GENIC	homozygous	108116374
1	59762669	59762670	G	A	19	GENIC	homozygous	108116375
1	59762724	59762725	G	A	22	GENIC	homozygous	108116376
1	59763065	59763066	C	T	20	GENIC	homozygous	108116377
1	59763145	59763146	A	C	24	GENIC	homozygous	108116378
1	59763668	59763669	G	T	27	GENIC	homozygous	108116379
1	59764459	59764460	C	T	17	GENIC	homozygous	108116380
1	59764579	59764580	G	A	19	GENIC	homozygous	108116381
1	59764637	59764638	C	G	19	GENIC	homozygous	108116382
1	59764841	59764842	C	A	24	GENIC	homozygous	108116383
1	59765043	59765044	G	A	25	GENIC	homozygous	108116384
1	59765838	59765839	A	G	22	GENIC	homozygous	108116385
1	59766911	59766912	A	C	24	GENIC	homozygous	108116386
1	59767131	59767132	C	T	30	GENIC	homozygous	108116387