chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	107129606	107129607	C		13	GENIC	possibly homozygous	138263169
8	107129673	107129674	T	C	22	GENIC	homozygous	138409685
8	107129765	107129766	C	T	31	GENIC	homozygous	138409686
8	107129767	107129768	T	C	31	GENIC	homozygous	138409687
8	107129801	107129802	C	T	29	GENIC	homozygous	138409688
8	107129804	107129805	G	A	29	GENIC	homozygous	138409689
8	107129852	107129853	G	T	35	GENIC	possibly homozygous	138409690
8	107129974	107129975	T	C	41	GENIC	homozygous	138409691
8	107130050	107130051	C	T	52	GENIC	homozygous	138409692
8	107130255	107130255		AAGA	45	GENIC	homozygous	138263170
8	107130444	107130445	T		48	GENIC	homozygous	138263171
8	107130518	107130519	A	G	56	GENIC	homozygous	138409693
8	107130532	107130533	A	G	58	GENIC	homozygous	138409694
8	107130707	107130708	C	T	49	GENIC	homozygous	138409695
8	107131055	107131056	A	G	38	GENIC	homozygous	138409696
8	107131082	107131083	G		37	GENIC	homozygous	138263172
8	107131222	107131223	A	G	35	GENIC	homozygous	138409697
8	107131690	107131690		CA	30	GENIC	possibly homozygous	138263173
8	107131767	107131769	AT		33	GENIC	possibly homozygous	138263174
8	107131794	107131794		CACA	37	GENIC	possibly homozygous	138263175
8	107131837	107131845	ACACTCAT		37	GENIC	possibly homozygous	138263176
8	107131907	107131907		ACAT	38	GENIC	homozygous	138263177
8	107132076	107132132	CACACACACACATACACACATACACACACATAGATTCACACACACACACACACACA		33	GENIC	homozygous	138263178
8	107132152	107132153	G	A	36	GENIC	homozygous	138409698
8	107132270	107132271	G	A	36	GENIC	possibly homozygous	138409699
8	107132271	107132272	C	T	36	GENIC	possibly homozygous	138409700
8	107132580	107132581	T	G	44	GENIC	possibly homozygous	138409701
8	107132659	107132660	G	A	40	GENIC	possibly homozygous	138409702
8	107132684	107132685	G	T	42	GENIC	possibly homozygous	138409703