chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	125522090	125522091	G	C	38	GENIC	homozygous	111696642
3	125522307	125522308	G	A	42	GENIC	homozygous	112394868
3	125522422	125522423	T	A	34	GENIC	homozygous	112394869
3	125522460	125522461	A	G	40	GENIC	homozygous	111696643
3	125522764	125522765	C	T	15	GENIC	homozygous	112394870
3	125522808	125522809	G	A	20	GENIC	homozygous	112394871
3	125522855	125522856	T	C	31	GENIC	homozygous	112394872
3	125523058	125523059	T	C	38	GENIC	homozygous	111696647
3	125525274	125525275	T	C	38	GENIC	homozygous	112359122
3	125526172	125526173	T	C	28	GENIC	homozygous	112359124
3	125526201	125526202	T	A	23	GENIC	homozygous	112394873
3	125526704	125526705	A	G	40	GENIC	homozygous	111696666
3	125527647	125527648	C	T	31	GENIC	homozygous	112359126
3	125527767	125527768	C	T	24	GENIC	homozygous	112359128
3	125528682	125528683	G	A	30	GENIC	homozygous	111696696
3	125528959	125528960	C	T	27	GENIC	homozygous	112359130
3	125529810	125529811	C	T	23	GENIC	homozygous	112359132
3	125529893	125529894	A	G	28	GENIC	homozygous	111696716
3	125530200	125530201	A	G	31	GENIC	homozygous	111696718
3	125530296	125530297	G	A	36	GENIC	homozygous	112359134
3	125530952	125530953	T	C	28	GENIC	homozygous	111696724
3	125531861	125531862	G	A	38	GENIC	homozygous	111696732
3	125531898	125531899	A	T	42	GENIC	homozygous	111696734
3	125532752	125532753	T	C	27	GENIC	homozygous	111696736
3	125545589	125545590	A	G	13	GENIC	homozygous	111696747
3	125545817	125545818	T	G	27	GENIC	homozygous	111696753
3	125545818	125545819	T	C	27	GENIC	homozygous	111696755
3	125545982	125545983	A	G	27	GENIC	homozygous	111696757
3	125546157	125546158	G	A	30	GENIC	homozygous	111696759
3	125546450	125546451	A	T	22	GENIC	homozygous	111696763
3	125547106	125547107	T	C	37	GENIC	homozygous	111696767
3	125547476	125547477	G	A	41	GENIC	homozygous	111696769
3	125547578	125547579	C	T	43	GENIC	homozygous	111696771