chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90711529	90711531	TG		14	GENIC	possibly homozygous	147296201
13	90780556	90780557	A	T	8	GENIC	homozygous	154786347
13	90780556	90780557	A		8	GENIC	heterozygous	403346025
13	90838245	90838246	C	T	33	GENIC	possibly homozygous	403346031
13	90838245	90838246	C		33	GENIC	heterozygous	403346032
13	90927440	90927442	TG		29	GENIC	heterozygous	139188661
13	90971189	90971190	G	C	8	GENIC	homozygous	403346035
13	90971189	90971190	G		8	GENIC	heterozygous	403346036
13	90992703	90992704	G		19	GENIC	homozygous	403346039
13	90992703	90992704	G	C	19	GENIC	heterozygous	403346040
13	90992705	90992706	G		19	GENIC	heterozygous	403346041
13	90992705	90992706	G	C	19	GENIC	homozygous	403346042
13	90946741	90946742	T		21	GENIC	heterozygous	141041760
13	90800505	90800506	G	T	2	GENIC	homozygous	147296894
13	90979322	90979323	A	T	10	GENIC	homozygous	139360071
13	91093241	91093242	A		42	GENIC	heterozygous	141143619
13	91201312	91201313	A		8	GENIC	heterozygous	139188799
13	91201312	91201313	A	G	8	GENIC	heterozygous	403346049
13	91201317	91201318	A		11	GENIC	heterozygous	144926096
13	91222723	91222727	TGTC		26	GENIC	homozygous	139188816
13	91252252	91252253	G		19	GENIC	heterozygous	403346052
13	91252252	91252253	G	T	19	GENIC	homozygous	403346053
13	91252256	91252257	G	T	21	GENIC	homozygous	403346054
13	91252256	91252257	G		21	GENIC	heterozygous	403346055
13	91252270	91252271	A	T	23	GENIC	homozygous	403346056
13	91252270	91252271	A		23	GENIC	heterozygous	403346057
13	91074414	91074415	T	C	52	GENIC	homozygous	143597051
13	91074463	91074464	C	T	48	GENIC	possibly homozygous	143597052