chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	108946621	108946622	T	C	28	GENIC	homozygous	112348273
3	108947626	108947627	A	G	9	GENIC	homozygous	111668896
3	108947627	108947628	C	G	9	GENIC	homozygous	111668897
3	108948768	108948769	C	T	20	GENIC	homozygous	112348275
3	108949312	108949313	G	A	33	GENIC	homozygous	112348277
3	108956597	108956598	A	G	23	GENIC	possibly homozygous	112348281
3	108957745	108957746	T	G	23	GENIC	homozygous	111668905
3	108960505	108960506	C	T	21	GENIC	homozygous	112348283
3	108960528	108960529	C	T	16	GENIC	homozygous	112348285
3	108964653	108964654	T	C	32	GENIC	homozygous	112348286
3	108965650	108965651	G	C	25	GENIC	possibly homozygous	112348288
3	108969775	108969776	C	T	23	GENIC	homozygous	112348290
3	108972558	108972559	C	T	29	GENIC	possibly homozygous	112348292
3	108974826	108974827	C	T	28	GENIC	possibly homozygous	112348294
3	108975685	108975686	C	T	22	GENIC	homozygous	111668913
3	108976369	108976370	C	T	16	GENIC	possibly homozygous	112348296