chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	45314965	45314966	G	A	45	GENIC	homozygous	114612620
13	45316453	45316454	G	A	37	GENIC	homozygous	114612621
13	45316617	45316618	C	G	29	GENIC	homozygous	114612622
13	45316659	45316660	A	G	29	GENIC	homozygous	114612623
13	45316772	45316776	CGGT		43	GENIC	possibly homozygous	131500794
13	45316777	45316778	G	A	43	GENIC	possibly homozygous	114612624
13	45316931	45316933	CG		28	GENIC	homozygous	131500795
13	45317069	45317070	C	T	35	GENIC	possibly homozygous	114612625
13	45317191	45317193	TT		31	GENIC	homozygous	131500796
13	45317216	45317216		T	30	GENIC	homozygous	131500797
13	45317279	45317280	A	G	36	GENIC	possibly homozygous	114612626
13	45317593	45317594	G	A	40	GENIC	homozygous	114612627
13	45317772	45317773	T	C	34	GENIC	homozygous	114612628
13	45317783	45317784	A		30	GENIC	homozygous	131500798
13	45318078	45318079	G	T	43	GENIC	homozygous	114612629
13	45318120	45318120		G	47	GENIC	homozygous	131500799
13	45318442	45318443	A	G	33	GENIC	homozygous	114612630
13	45318731	45318732	G	T	52	GENIC	homozygous	114612631