chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47589319	47589319		T	16	GENIC	homozygous	129050751
13	47589328	47589329	A		13	GENIC	homozygous	129050752
13	47589335	47589335		A	14	GENIC	homozygous	129050753
13	47589399	47589399		G	24	GENIC	homozygous	129050754
13	47589401	47589401		TG	23	GENIC	homozygous	129050755
13	47589431	47589431		GTC	24	GENIC	homozygous	129050756
13	47589454	47589454		G	23	GENIC	homozygous	129050757
13	47589474	47589475	A		25	GENIC	homozygous	129050758
13	47589481	47589481		A	27	GENIC	homozygous	129050759
13	47589567	47589567		T	24	GENIC	homozygous	129050760
13	47589575	47589575		G	25	GENIC	homozygous	129050761
13	47589600	47589600		G	24	GENIC	homozygous	129050762
13	47589602	47589603	A	T	27	GENIC	homozygous	114337816
13	47589640	47589641	T	A	24	GENIC	homozygous	114337818
13	47589702	47589702		C	28	GENIC	homozygous	129050763
13	47589777	47589778	T		37	GENIC	homozygous	129050764
13	47589780	47589781	G		37	GENIC	homozygous	129050765
13	47589935	47589935		C	21	GENIC	homozygous	129050766