chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243160871	243160872	A	C	54	GENIC	homozygous	110345902
2	243163706	243163707	T	C	56	GENIC	homozygous	110345904
2	243163778	243163779	C	T	58	GENIC	possibly homozygous	110345906
2	243163932	243163933	A	G	43	GENIC	homozygous	110345908
2	243164927	243164928	A	T	67	GENIC	homozygous	110345910
2	243165800	243165801	T	C	43	GENIC	homozygous	110345912
2	243165974	243165975	C	A	55	GENIC	homozygous	110345914
2	243166444	243166445	T	C	42	GENIC	homozygous	110345916
2	243166527	243166528	C	T	49	GENIC	homozygous	110345918
2	243167540	243167541	T	C	65	GENIC	homozygous	110345922
2	243167850	243167851	A	T	56	GENIC	homozygous	110345924
2	243168001	243168002	G	A	43	GENIC	homozygous	110345926
2	243165029	243165033	TTTC		43	GENIC	homozygous	127756889
2	243167922	243167922		A	48	GENIC	homozygous	127756890
2	243167922	243167923	G	A	46	GENIC	homozygous	120131759
2	243168823	243168824	G	A	50	GENIC	homozygous	110345928
2	243168920	243168925	TAGTA		50	GENIC	homozygous	127756891
2	243169511	243169512	C	G	49	GENIC	homozygous	110345930
2	243170265	243170266	A	G	61	GENIC	homozygous	110345932
2	243170706	243170707	A	T	31	GENIC	homozygous	110345934
2	243170719	243170720	G	A	26	GENIC	homozygous	111032608
2	243170720	243170721	C	T	26	GENIC	homozygous	111032610
2	243170722	243170723	G	A	27	GENIC	homozygous	111032612
2	243170801	243170802	T	C	38	GENIC	possibly homozygous	110345936
2	243170735	243170736	A	G	23	GENIC	homozygous	121620845
2	243170759	243170760	T	C	25	GENIC	homozygous	110845327
2	243170773	243170774	A	G	29	GENIC	possibly homozygous	110633125
2	243170816	243170817	G	C	40	GENIC	possibly homozygous	110345938
2	243171900	243171901	A	C	79	GENIC	homozygous	110345940