chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	114506146	114506147	A	AC	18	GENIC	possibly homozygous	52824004
8	114506160	114506161	T	TAC	5	GENIC	heterozygous	53410877
8	114506160	114506161	T	TACACAC	5	GENIC	heterozygous	53410879
8	114506910	114506911	T	C	31	GENIC	homozygous	52824005
8	114507453	114507454	C	A	24	GENIC	homozygous	52824006
8	114507589	114507590	T	TA	20	GENIC	possibly homozygous	52824007
8	114508144	114508145	C	CTCTG	17	GENIC	homozygous	52824008
8	114508295	114508296	G	GGC	21	GENIC	homozygous	53410881
8	114508299	114508300	C	CCT	20	GENIC	homozygous	53410882
8	114508301	114508303	AA	--	21	GENIC	homozygous	53410883
8	114508304	114508306	GA	--	21	GENIC	homozygous	52824009
8	114509221	114509224	AAG	---	13	GENIC	homozygous	52824011
8	114509499	114509502	AAA	---	12	GENIC	heterozygous	53047751
8	114509500	114509502	AA	--	12	GENIC	heterozygous	52824012
8	114512075	114512076	G	C	20	GENIC	homozygous	52824013
8	114512505	114512506	T	TA	14	GENIC	possibly homozygous	52824014
8	114514208	114514209	G	A	20	GENIC	homozygous	52824015
8	114514342	114514343	T	TG	8	GENIC	possibly homozygous	52824016