chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	118890556	118890557	T	G	31	GENIC	homozygous	117062257
8	118890666	118890667	T	C	28	GENIC	homozygous	116674810
8	118890799	118890800	T	C	28	GENIC	homozygous	117062259
8	118890836	118890837	G	T	30	GENIC	possibly homozygous	117062261
8	118890941	118890942	A	G	44	GENIC	homozygous	117062263
8	118890956	118890957	C	T	38	GENIC	homozygous	117062265
8	118891093	118891094	A	C	36	GENIC	possibly homozygous	117062267
8	118891448	118891449	A	G	26	GENIC	homozygous	117062269
8	118891657	118891658	C	T	35	GENIC	homozygous	117062271
8	118891678	118891679	C	T	33	GENIC	homozygous	117062273
8	118891804	118891805	T	C	41	GENIC	homozygous	117062275
8	118891950	118891951	T	A	41	GENIC	homozygous	117062277
8	118892525	118892526	G	A	33	GENIC	homozygous	117062279
8	118892603	118892604	C	T	45	GENIC	homozygous	116674812
8	118892697	118892698	T	G	36	GENIC	homozygous	117062281
8	118892746	118892747	T	C	36	GENIC	homozygous	117062283
8	118893017	118893018	C	A	61	GENIC	homozygous	117062285
8	118893235	118893236	C	G	29	GENIC	homozygous	117062287
8	118893423	118893424	G	A	30	GENIC	homozygous	117062289
8	118893433	118893434	T	C	32	GENIC	homozygous	117062291