chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	96341802	96341803	G	GAAA	26	GENIC	possibly homozygous	50145371
13	96341802	96341803	G	GAA	26	GENIC	heterozygous	50585417
13	96341919	96341920	A	G	32	GENIC	possibly homozygous	49968175
13	96342150	96342151	C	CA	31	GENIC	homozygous	49861332
13	96342307	96342308	A	AAAGTCCTAC	35	GENIC	homozygous	49861333
13	96342478	96342479	T	G	31	GENIC	homozygous	49968177
13	96343056	96343057	C	T	26	GENIC	homozygous	50145373
13	96343376	96343377	G	GGT	3	GENIC	homozygous	50585418
13	96343772	96343773	A	G	27	GENIC	possibly homozygous	49968180
13	96343970	96343971	C	T	36	GENIC	homozygous	50145375
13	96344817	96344818	T	TCCCACC	7	GENIC	homozygous	50585419