chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	32961838	32961839	A	C	4	GENIC	homozygous	122952029
8	32961845	32961846	A	C	4	GENIC	homozygous	122952030
8	32961849	32961850	G	C	4	GENIC	homozygous	122952031
8	32961855	32961856	G	T	4	GENIC	homozygous	122952032
8	32961861	32961862	A	T	4	GENIC	homozygous	122952033
8	32961874	32961875	A	T	3	GENIC	homozygous	130770958
8	32998226	32998227	C		18	GENIC	homozygous	128580060
8	32998246	32998246		C	21	GENIC	homozygous	128580061
8	32998251	32998251		G	21	GENIC	homozygous	128580062
8	32998266	32998266		T	23	GENIC	homozygous	128580063
8	32998281	32998281		G	26	GENIC	homozygous	128580064
8	32998284	32998285	G	T	23	GENIC	homozygous	116449231
8	32998288	32998288		T	23	GENIC	homozygous	128580065
8	32998312	32998313	C		18	GENIC	homozygous	128580066
8	32998342	32998342		G	19	GENIC	homozygous	128580067
8	32998356	32998356		A	21	GENIC	homozygous	128580068
8	32998378	32998378		T	18	GENIC	homozygous	128580069
8	32998388	32998389	A	G	18	GENIC	homozygous	116449232
8	32998414	32998414		T	20	GENIC	homozygous	128580070
8	32998425	32998426	G	T	17	GENIC	homozygous	116449233
8	32998437	32998438	A	C	18	GENIC	homozygous	116449234
8	32998439	32998440	C		18	GENIC	homozygous	128580071
8	32998472	32998473	G		16	GENIC	homozygous	128580072
8	32998487	32998487		T	17	GENIC	homozygous	128580073
8	32998491	32998492	G	C	15	GENIC	homozygous	116449235
8	32998513	32998513		CCC	11	GENIC	homozygous	128580074
8	32999332	32999333	C		15	GENIC	homozygous	128580075
8	32999333	32999334	C	A	15	GENIC	homozygous	117916140
8	32998288	32998289	G	A	23	GENIC	homozygous	117916136
8	32998407	32998408	A	G	20	GENIC	homozygous	117916137
8	32998408	32998409	G	T	20	GENIC	homozygous	117916138
8	32998410	32998411	G	T	20	GENIC	homozygous	117916139
8	33008150	33008151	A		10	GENIC	homozygous	128580082