chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	119129352	119129353	T	G	33	GENIC	homozygous	109994880
2	119129928	119129929	T	C	49	GENIC	homozygous	109994882
2	119131472	119131473	C	A	42	GENIC	homozygous	109994884
2	119132298	119132299	T	A	18	GENIC	homozygous	109994886
2	119133279	119133280	T	C	31	GENIC	homozygous	109994888
2	119135046	119135047	C	T	28	GENIC	homozygous	109994892
2	119135075	119135076	T	G	24	GENIC	homozygous	109994894
2	119135400	119135401	G	A	21	GENIC	homozygous	109994896
2	119135667	119135668	G	A	24	GENIC	homozygous	109994898
2	119135883	119135884	A	T	42	GENIC	possibly homozygous	109994900
2	119135929	119135930	C	T	47	GENIC	possibly homozygous	109994902
2	119136339	119136340	A	G	23	GENIC	homozygous	109994904
2	119137039	119137040	T	C	31	GENIC	homozygous	109994906
2	119137056	119137057	T	C	31	GENIC	homozygous	109994908
2	119137155	119137156	G	A	27	GENIC	homozygous	109994910
2	119137197	119137198	G	A	30	GENIC	homozygous	109994912
2	119137338	119137339	T	C	27	GENIC	homozygous	109994914
2	119137469	119137470	C	T	25	GENIC	possibly homozygous	109994915
2	119137483	119137484	A	G	26	GENIC	possibly homozygous	109994917
2	119137792	119137793	T	C	25	GENIC	homozygous	109994919
2	119138888	119138889	G	A	30	GENIC	homozygous	109994923
2	119138961	119138962	T	C	35	GENIC	homozygous	109994925
2	119139443	119139444	A	T	17	GENIC	homozygous	109994927