chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243160871	243160872	A	C	16	GENIC	homozygous	110345902
2	243163706	243163707	T	C	29	GENIC	homozygous	110345904
2	243163778	243163779	C	T	23	GENIC	homozygous	110345906
2	243163932	243163933	A	G	26	GENIC	homozygous	110345908
2	243164927	243164928	A	T	32	GENIC	possibly homozygous	110345910
2	243165800	243165801	T	C	20	GENIC	homozygous	110345912
2	243165974	243165975	C	A	27	GENIC	homozygous	110345914
2	243166444	243166445	T	C	21	GENIC	homozygous	110345916
2	243166527	243166528	C	T	26	GENIC	homozygous	110345918
2	243167540	243167541	T	C	25	GENIC	homozygous	110345922
2	243167850	243167851	A	T	19	GENIC	homozygous	110345924
2	243168001	243168002	G	A	23	GENIC	homozygous	110345926
2	243165029	243165033	TTTC		24	GENIC	homozygous	127756889
2	243167922	243167922		A	21	GENIC	homozygous	127756890
2	243167922	243167923	G	A	21	GENIC	homozygous	120131759
2	243168823	243168824	G	A	31	GENIC	homozygous	110345928
2	243169511	243169512	C	G	27	GENIC	homozygous	110345930
2	243170265	243170266	A	G	21	GENIC	homozygous	110345932
2	243170706	243170707	A	T	14	GENIC	homozygous	110345934
2	243168920	243168925	TAGTA		26	GENIC	homozygous	127756891
2	243170719	243170720	G	A	12	GENIC	homozygous	111032608
2	243170720	243170721	C	T	12	GENIC	homozygous	111032610
2	243170722	243170723	G	A	11	GENIC	homozygous	111032612
2	243170735	243170736	A	G	10	GENIC	homozygous	121620845
2	243170759	243170760	T	C	9	GENIC	homozygous	110845327
2	243170773	243170774	A	G	8	GENIC	homozygous	110633125
2	243170801	243170802	T	C	8	GENIC	homozygous	110345936
2	243170816	243170817	G	C	11	GENIC	homozygous	110345938
2	243171900	243171901	A	C	26	GENIC	homozygous	110345940