chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	88056895	88056896	T	C	37	GENIC	homozygous	115188840
13	88056901	88056902	G	A	37	GENIC	homozygous	118502949
13	88057431	88057432	A	G	38	GENIC	homozygous	118502950
13	88057445	88057446	T	A	47	GENIC	homozygous	118502951
13	88057578	88057579	T	C	45	GENIC	homozygous	118502952
13	88057905	88057906	G	C	15	GENIC	homozygous	118502953
13	88058237	88058238	A	G	31	GENIC	homozygous	118502954
13	88058377	88058378	A	T	32	GENIC	possibly homozygous	118502955
13	88058659	88058660	A	G	43	GENIC	homozygous	115188850
13	88058889	88058890	G	T	41	GENIC	homozygous	118502956
13	88059058	88059059	C	T	21	GENIC	possibly homozygous	118502957
13	88059132	88059133	G	A	26	GENIC	homozygous	118502958
13	88059328	88059329	A	T	32	GENIC	homozygous	118502959
13	88059399	88059400	A	C	44	GENIC	possibly homozygous	115188854
13	88059553	88059554	A	C	38	GENIC	homozygous	118502960
13	88059738	88059739	T	C	41	GENIC	homozygous	115188860
13	88059781	88059782	G	A	39	GENIC	homozygous	118502961
13	88059789	88059790	T	C	36	GENIC	homozygous	118502962
13	88059920	88059921	C	T	35	GENIC	homozygous	118502963
13	88059965	88059966	C	G	43	GENIC	homozygous	115188862
13	88059976	88059977	G	A	38	GENIC	homozygous	115188864
13	88060046	88060047	T	C	38	GENIC	homozygous	115188866