chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	237969718	237969719	T	C	18	GENIC	homozygous	110840664
2	237969858	237969859	G	A	6	GENIC	homozygous	110840665
2	237969897	237969898	C	T	7	GENIC	homozygous	110840666
2	237969985	237969986	T	C	11	GENIC	homozygous	110840667
2	237970717	237970718	G	C	20	GENIC	homozygous	110325532
2	237970989	237970990	G	A	16	GENIC	homozygous	110325534
2	237971066	237971067	G	A	19	GENIC	homozygous	110840669
2	237971664	237971665	A	T	23	GENIC	homozygous	110840670
2	237971911	237971912	A	G	14	GENIC	homozygous	110840671
2	237971949	237971950	T	C	21	GENIC	homozygous	110840672
2	237971965	237971966	A	T	14	GENIC	homozygous	110840673
2	237972014	237972015	T	C	9	GENIC	homozygous	110840674
2	237972197	237972198	T	C	12	GENIC	homozygous	110325540
2	237972439	237972440	C	T	29	GENIC	homozygous	110840675
2	237972483	237972484	T	C	18	GENIC	homozygous	110325542
2	237973470	237973471	C	A	7	GENIC	homozygous	110840676
2	237973476	237973477	T	G	8	GENIC	homozygous	110840677
2	237973537	237973538	G	A	15	GENIC	homozygous	110840678
2	237974034	237974035	C	T	15	GENIC	homozygous	110840679
2	237974338	237974339	C	G	6	GENIC	heterozygous	110325544
2	237974435	237974436	T	C	17	GENIC	homozygous	110840680