chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	49951308	49951309	A	ATG	11	GENIC	heterozygous	54379979
6	49951308	49951309	A	ATGTG	11	GENIC	heterozygous	54379981
6	49952662	49952663	T	A	23	GENIC	homozygous	54379983
6	49952663	49952664	A	T	22	GENIC	homozygous	54379985
6	49953232	49953233	G	A	28	GENIC	homozygous	54379987
6	49953264	49953265	A	G	32	GENIC	homozygous	54379989
6	49953600	49953601	G	T	22	GENIC	homozygous	54379991
6	49953689	49953690	T	C	34	GENIC	homozygous	54379993
6	49954160	49954161	C	T	30	GENIC	homozygous	54379995
6	49954672	49954673	T	TTGTCCAGTATG	28	GENIC	homozygous	54379997
6	49954677	49954678	C	CT	23	GENIC	homozygous	54379999
6	49955058	49955059	T	C	40	GENIC	homozygous	54380001
6	49956794	49956795	T	G	29	GENIC	homozygous	54380003