chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	148910272	148910273	C	G	26	GENIC	homozygous	111771095
3	148912415	148912416	G	T	26	GENIC	homozygous	111771097
3	148915810	148915811	A	G	21	GENIC	homozygous	111771099
3	148916162	148916163	T	C	16	GENIC	homozygous	111771101
3	148916263	148916264	A	G	25	GENIC	homozygous	111771103
3	148917269	148917270	C	T	26	GENIC	homozygous	111771105
3	148919432	148919433	G	A	19	GENIC	homozygous	111771107
3	148920617	148920618	A	G	24	GENIC	homozygous	111771109
3	148921262	148921263	A	G	24	GENIC	homozygous	111771111
3	148925614	148925615	G	A	31	GENIC	homozygous	111771113
3	148925969	148925970	G	T	20	GENIC	homozygous	111771117
3	148927260	148927261	A	G	20	GENIC	homozygous	111771119
3	148928094	148928095	C	T	27	GENIC	homozygous	111771121
3	148928234	148928235	T	C	30	GENIC	homozygous	111771123
3	148928600	148928601	A	C	18	GENIC	homozygous	111771125
3	148929130	148929131	T	C	15	GENIC	homozygous	111771127
3	148932218	148932219	C	T	17	GENIC	homozygous	111771129
3	148934387	148934388	G	A	24	GENIC	homozygous	111771131
3	148937058	148937059	A	C	30	GENIC	homozygous	111771135
3	148937586	148937587	T	G	17	GENIC	homozygous	111771137
3	148939520	148939521	T	C	17	GENIC	homozygous	111771139