chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	11317694	11317695	G	T	14	GENIC	homozygous	111875644
3	11320202	11320203	T	A	26	GENIC	homozygous	111446664
3	11320491	11320492	T	C	44	GENIC	homozygous	111446668
3	11322406	11322407	C	A	33	GENIC	homozygous	111875646
3	11322536	11322537	T	C	32	GENIC	homozygous	111446670
3	11325522	11325523	G	A	27	GENIC	homozygous	111446676
3	11328249	11328250	T	C	34	GENIC	homozygous	111446678
3	11328751	11328752	T	C	31	GENIC	homozygous	111446680
3	11329157	11329158	A	G	27	GENIC	homozygous	111446682
3	11329432	11329433	A	G	12	GENIC	homozygous	111446686
3	11329487	11329488	G	A	20	GENIC	heterozygous	111875648
3	11331014	11331015	G	T	22	GENIC	homozygous	111446694
3	11331277	11331278	A	G	24	GENIC	homozygous	111446696
3	11331707	11331708	A	G	23	GENIC	homozygous	111446698
3	11331852	11331853	G	A	25	GENIC	homozygous	111446700
3	11332167	11332168	T	G	39	GENIC	homozygous	111446702
3	11332193	11332194	T	C	36	GENIC	homozygous	111446704
3	11332800	11332801	A	G	31	GENIC	homozygous	111446706
3	11334928	11334929	G	A	39	GENIC	homozygous	111875650
3	11335172	11335173	C	A	42	GENIC	homozygous	111875652
3	11335419	11335420	A	G	26	GENIC	homozygous	111446712
3	11337371	11337372	C	T	34	GENIC	homozygous	111875654