chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	97439686	97439687	T	C	54	GENIC	homozygous	116592278
8	97439699	97439700	G	A	52	GENIC	homozygous	116592280
8	97441281	97441282	C	T	54	GENIC	homozygous	116592282
8	97441725	97441726	A	T	49	GENIC	homozygous	116592284
8	97442262	97442263	T	G	51	GENIC	homozygous	116592286
8	97443023	97443024	C	T	44	GENIC	homozygous	116592288
8	97443280	97443281	C	T	46	GENIC	homozygous	116592290
8	97443319	97443320	C	T	46	GENIC	homozygous	116592292
8	97443320	97443321	A	G	45	GENIC	homozygous	116592294
8	97442575	97442575		A	41	GENIC	homozygous	128618786
8	97443496	97443502	ATCCCC		40	GENIC	homozygous	128618787
8	97443504	97443504		GGGG	41	GENIC	homozygous	128618788
8	97444031	97444032	T	C	6	GENIC	heterozygous	118077517
8	97445847	97445848	A	G	33	GENIC	homozygous	116592296
8	97446141	97446142	C	T	51	GENIC	homozygous	116592298
8	97447924	97447925	T	C	20	GENIC	homozygous	116592300
8	97450523	97450524	G	A	42	GENIC	homozygous	116592302
8	97450721	97450722	C	T	46	GENIC	homozygous	116592304
8	97451630	97451631	G	A	39	GENIC	homozygous	116592306
8	97451807	97451807		G	40	GENIC	homozygous	128618789
8	97452695	97452695		CAACCACAGACCAAA	34	GENIC	homozygous	128618790
8	97454242	97454243	A	G	53	GENIC	homozygous	116592308
8	97455868	97455869	T		32	GENIC	homozygous	128618791
8	97456680	97456681	T		45	GENIC	possibly homozygous	128618792
8	97457351	97457393	TAGCAAGACCCCCTCATAAGATCCCAGGTCCCAACGAGTCTG		39	GENIC	homozygous	128618793
8	97457852	97457853	C	G	56	GENIC	homozygous	116592310