chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	45316617	45316618	C	G	57	GENIC	homozygous	114612622
13	45316659	45316660	A	G	55	GENIC	homozygous	114612623
13	45316772	45316776	CGGT		49	GENIC	homozygous	131500794
13	45316777	45316778	G	A	50	GENIC	homozygous	114612624
13	45316931	45316933	CG		36	GENIC	homozygous	131500795
13	45317191	45317193	TT		50	GENIC	homozygous	131500796
13	45317279	45317280	A	G	46	GENIC	homozygous	114612626
13	45317772	45317773	T	C	53	GENIC	homozygous	114612628
13	45317783	45317784	A		54	GENIC	homozygous	131500798
13	45318442	45318443	A	G	62	GENIC	possibly homozygous	114612630
13	45318731	45318732	G	T	48	GENIC	homozygous	114612631
13	45318477	45318478	G	C	68	GENIC	possibly homozygous	114756075
13	45317223	45317223		C	42	GENIC	homozygous	133260256