chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	32637298	32637299	T	A	49	GENIC	homozygous	108068564
1	32637422	32637423	G	A	53	GENIC	homozygous	108068565
1	32638228	32638229	C	A	9	GENIC	homozygous	127528922
1	32638242	32638242		G	2	GENIC	homozygous	127370417
1	32638281	32638282	C		8	GENIC	homozygous	127370418
1	32638291	32638292	C		17	GENIC	homozygous	127370419
1	32638329	32638329		T	28	GENIC	homozygous	127370420
1	32638332	32638332		G	32	GENIC	homozygous	127370421
1	32638336	32638337	G		32	GENIC	homozygous	127370422
1	32638377	32638378	A		43	GENIC	homozygous	127370423
1	32638385	32638386	C		45	GENIC	homozygous	127370424
1	32638403	32638404	C		47	GENIC	homozygous	127370425
1	32638437	32638437		G	43	GENIC	homozygous	127370426
1	32639723	32639724	T	A	57	GENIC	homozygous	108068566
1	32640414	32640415	A	T	76	GENIC	possibly homozygous	108068567
1	32641349	32641350	C	T	77	GENIC	homozygous	108068568
1	32642283	32642284	T	C	57	GENIC	homozygous	108068569
1	32642318	32642319	T	G	48	GENIC	homozygous	108068570
1	32643473	32643474	G	A	39	GENIC	homozygous	108068571
1	32644936	32644937	A	G	47	GENIC	homozygous	108068573
1	32644485	32644486	C	T	65	GENIC	homozygous	108068572