chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	115255969	115255970	G	A	21	GENIC	homozygous	144316210
2	115256891	115256892	A	G	13	GENIC	homozygous	144316211
2	115258001	115258001		AAA	21	GENIC	homozygous	144275976
2	115258556	115258557	T	C	14	GENIC	homozygous	144316212
2	115260678	115260679	G	A	14	GENIC	homozygous	144316214
2	115261175	115261175		CCA	25	GENIC	homozygous	144275977
2	115261430	115261431	A	G	12	GENIC	homozygous	144316215
2	115261931	115261932	G	T	19	GENIC	homozygous	144316216
2	115262035	115262036	C	T	14	GENIC	homozygous	144316217
2	115262691	115262691		G	12	GENIC	homozygous	144275978
2	115264149	115264151	TT		24	GENIC	homozygous	144275979
2	115265974	115265975	G	T	14	GENIC	homozygous	144316218
2	115267647	115267648	G	A	19	GENIC	homozygous	144316219
2	115267828	115267828		T	12	GENIC	homozygous	144275980
2	115268146	115268147	G	A	21	GENIC	homozygous	144316220
2	115268374	115268375	C	G	21	GENIC	homozygous	144316221
2	115269175	115269176	A	G	16	GENIC	homozygous	144316222
2	115269436	115269437	T	G	20	GENIC	homozygous	136264751
2	115260583	115260583		GC	14	GENIC	possibly homozygous	140859370
2	115263138	115263139	G	A	9	GENIC	homozygous	153981767
2	115265460	115265460		T	4	GENIC	homozygous	141086241