chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	127736100	127736101	C	T	28	GENIC	homozygous	116719004
8	127736584	127736585	T	C	31	GENIC	homozygous	116719006
8	127736774	127736775	G	A	38	GENIC	homozygous	116719008
8	127738087	127738088	A	G	41	GENIC	homozygous	116719016
8	127743502	127743503	T	C	24	GENIC	homozygous	116719022
8	127744014	127744015	A	G	28	GENIC	homozygous	116719024
8	127744602	127744603	A	G	40	GENIC	homozygous	116719026
8	127745043	127745044	A	G	30	GENIC	homozygous	116719028
8	127745433	127745434	T	C	34	GENIC	homozygous	116719030
8	127747240	127747241	A	C	38	GENIC	homozygous	116719032
8	127747438	127747439	A	C	34	GENIC	homozygous	116719034
8	127747495	127747496	A	C	27	GENIC	homozygous	116719036
8	127749065	127749066	T	A	31	GENIC	homozygous	116719038
8	127749509	127749510	T	C	21	GENIC	homozygous	116719040
8	127751020	127751021	G	A	15	GENIC	homozygous	116719044
8	127751842	127751843	G	A	34	GENIC	homozygous	116719046
8	127752806	127752807	G	C	30	GENIC	homozygous	116719048