chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	108643365	108643366	A	G	47	GENIC	homozygous	138411637
8	108644703	108644704	G	C	41	GENIC	possibly homozygous	154538853
8	108645322	108645323	A	G	57	GENIC	homozygous	138411641
8	108646839	108646840	A	G	15	GENIC	homozygous	138411642
8	108647971	108647972	A	G	61	GENIC	homozygous	138411644
8	108651422	108651423	A	G	44	GENIC	homozygous	138411650
8	108657879	108657880	C	T	38	GENIC	homozygous	138411667
8	108658997	108658998	G	A	47	GENIC	homozygous	138411669
8	108660326	108660327	A	G	57	GENIC	homozygous	142099633
8	108649485	108649485		G	56	GENIC	homozygous	138263705
8	108644703	108644704	G		41	GENIC	heterozygous	404081237
8	108648949	108648950	C	T	55	GENIC	homozygous	142099626
8	108658166	108658167	C	T	57	GENIC	homozygous	142099627
8	108658549	108658550	A	T	16	GENIC	homozygous	142099628
8	108658823	108658824	C	G	66	GENIC	homozygous	142099630
8	108659255	108659256	C	G	57	GENIC	homozygous	142099631
8	108659776	108659777	G	C	62	GENIC	homozygous	142099632
8	108660511	108660512	A	G	72	GENIC	homozygous	142099634
8	108660526	108660527	C	T	74	GENIC	homozygous	142099635
8	108661074	108661074		TCCCCTC	63	GENIC	homozygous	142030306
8	108661106	108661107	A	G	63	GENIC	homozygous	138411673
8	108661450	108661451	A	T	60	GENIC	homozygous	138411674