chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	96222376	96222377	A	G	30	GENIC	homozygous	114790940
13	96222799	96222800	C	A	42	GENIC	homozygous	115155060
13	96223166	96223167	T	C	22	GENIC	homozygous	114790942
13	96224575	96224576	T	C	27	GENIC	homozygous	114790944
13	96225439	96225440	A	T	29	GENIC	homozygous	114790946
13	96225440	96225441	C	T	29	GENIC	homozygous	114790948
13	96225482	96225483	G	A	22	GENIC	homozygous	114790950
13	96226839	96226840	T	G	28	GENIC	homozygous	114790952
13	96226932	96226933	T	C	29	GENIC	homozygous	114790954
13	96228564	96228565	G	A	39	GENIC	homozygous	114790956
13	96231525	96231526	A	G	36	GENIC	homozygous	114790958
13	96233342	96233343	T	G	31	GENIC	homozygous	114790960
13	96233722	96233723	T	C	42	GENIC	homozygous	114790962
13	96234543	96234544	A	T	31	GENIC	homozygous	114790964
13	96237897	96237898	G	A	23	GENIC	homozygous	114790966
13	96225432	96225437	TAAAA		29	GENIC	homozygous	131136002
13	96228081	96228083	AT		43	GENIC	homozygous	131136003
13	96237033	96237034	G		16	GENIC	homozygous	131136004
13	96227304	96227305	A	G	24	GENIC	homozygous	115224050