chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	26893363	26893364	C	T	34	GENIC	homozygous	109154039
20	26900358	26900359	G	A	47	GENIC	homozygous	109154041
20	26900377	26900378	C	G	41	GENIC	homozygous	109154043
20	26900692	26900693	C	T	25	GENIC	homozygous	109154045
20	26901100	26901101	C	T	42	GENIC	homozygous	109154047
20	26904575	26904576	A	T	31	GENIC	homozygous	109154049
20	26904946	26904947	A	G	51	GENIC	homozygous	109154051
20	26906401	26906402	T	A	35	GENIC	homozygous	109154053
20	26906613	26906614	C	G	35	GENIC	homozygous	109154055
20	26907322	26907323	G	A	31	GENIC	homozygous	109154057
20	26907471	26907472	G	A	39	GENIC	homozygous	109154059
20	26907965	26907966	G	A	21	GENIC	homozygous	109154061
20	26910368	26910369	C	T	41	GENIC	homozygous	109154063
20	26910608	26910609	T	C	44	GENIC	homozygous	109154065
20	26910799	26910800	G	A	32	GENIC	homozygous	109154067
20	26911243	26911244	G	A	36	GENIC	homozygous	109154069
20	26911406	26911407	C	T	48	GENIC	homozygous	109154071