chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	133930091	133930092	C	T	32	GENIC	homozygous	118983112
5	133931771	133931772	A	G	15	GENIC	homozygous	114015173
5	133932583	133932584	G	A	15	GENIC	homozygous	114143374
5	133933383	133933384	T	C	29	GENIC	homozygous	114143375
5	133934338	133934339	T	C	33	GENIC	homozygous	114015175
5	133945596	133945597	G	A	11	GENIC	homozygous	114143378
5	133946754	133946755	A	T	39	GENIC	homozygous	114143379
5	133947140	133947141	C	A	33	GENIC	homozygous	114143380
5	133947231	133947232	T	C	37	GENIC	homozygous	114015179
5	133947627	133947628	T	C	29	GENIC	homozygous	114015180
5	133949653	133949654	A	G	16	GENIC	homozygous	114015181
5	133949654	133949655	A	G	16	GENIC	homozygous	114015182
5	133950589	133950590	A	G	25	GENIC	homozygous	114143381
5	133951146	133951147	A	C	29	GENIC	homozygous	114015183
5	133956027	133956028	A	G	21	GENIC	homozygous	114143382
5	133956353	133956354	T	A	24	GENIC	homozygous	114143384