chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	108891955	108891956	T		45	GENIC	homozygous	138263775
8	108894248	108894249	G	A	63	GENIC	possibly homozygous	142099766
8	108897310	108897311	T	C	55	GENIC	homozygous	138411937
8	108903614	108903617	AGA		49	GENIC	homozygous	138263780
8	108903723	108903724	A	G	49	GENIC	homozygous	138411941
8	108904003	108904004	G	A	53	GENIC	homozygous	138411942
8	108905703	108905704	A	G	63	GENIC	homozygous	138411944
8	108905997	108905998	G	A	49	GENIC	homozygous	142099767
8	108911961	108911962	C	T	40	GENIC	homozygous	142099768
8	108923505	108923505		T	45	GENIC	homozygous	138263787
8	108924015	108924016	A		54	GENIC	homozygous	138263788
8	108926797	108926798	T	A	17	GENIC	homozygous	138411952
8	108927914	108927915	A	G	37	GENIC	homozygous	138411953
8	108915096	108915112	GCCTAGCAACCGCGAG		37	GENIC	homozygous	142030340
8	108920815	108920816	T		21	GENIC	heterozygous	138263786
8	108920815	108920816	T	G	21	GENIC	homozygous	154539821
8	108928904	108928905	T	A	51	GENIC	homozygous	142099769
8	108928961	108928962	C	T	41	GENIC	possibly homozygous	142099770
8	108932401	108932402	G	A	40	GENIC	homozygous	142099771
8	108936166	108936167	A	G	53	GENIC	homozygous	138411959
8	108942648	108942649	C	T	40	GENIC	homozygous	142099772
8	108943774	108943775	G	C	14	GENIC	heterozygous	403248652
8	108935260	108935261	T		21	GENIC	homozygous	403248644
8	108935260	108935261	T	A	21	GENIC	heterozygous	403248645
8	108943768	108943769	G		13	GENIC	heterozygous	403248646
8	108943768	108943769	G	C	13	GENIC	heterozygous	403248647
8	108943770	108943771	G		14	GENIC	heterozygous	403248648
8	108943770	108943771	G	C	14	GENIC	heterozygous	403248649
8	108943772	108943773	G		31	GENIC	heterozygous	403248650
8	108943772	108943773	G	C	31	GENIC	possibly homozygous	403248651
8	108943774	108943775	G		14	GENIC	heterozygous	403248653
8	108947169	108947170	A		47	GENIC	homozygous	138263798
8	108942691	108942692	A		18	GENIC	heterozygous	141017266