chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	15659226	15659227	C	T	49	GENIC	homozygous	136643510
3	15659844	15659845	G	A	67	GENIC	homozygous	136643511
3	15664711	15664712	T	G	68	GENIC	homozygous	136643512
3	15664795	15664796	A	G	59	GENIC	homozygous	136643513
3	15667207	15667208	G	A	73	GENIC	homozygous	136643514
3	15667317	15667318	C	T	65	GENIC	homozygous	136643515
3	15667327	15667328	T	C	70	GENIC	homozygous	136643516
3	15667434	15667435	C	T	71	GENIC	homozygous	136643517
3	15667658	15667659	A	G	62	GENIC	homozygous	136643518
3	15667879	15667880	A	G	43	GENIC	homozygous	136643519
3	15668136	15668137	T	C	42	GENIC	homozygous	136643520
3	15668608	15668609	C	T	58	GENIC	homozygous	136643521
3	15669312	15669313	G	A	85	GENIC	homozygous	136643522
3	15669425	15669426	T	A	54	GENIC	possibly homozygous	136643523
3	15669980	15669981	G	C	79	GENIC	homozygous	136643524
3	15670433	15670434	G	A	79	GENIC	homozygous	136643525
3	15671527	15671528	T	G	50	GENIC	homozygous	136643526
3	15672004	15672005	G	A	50	GENIC	homozygous	136643527
3	15672684	15672685	A	G	65	GENIC	homozygous	136643528
3	15673026	15673027	T	G	46	GENIC	homozygous	136643529
3	15673250	15673251	A	G	40	GENIC	homozygous	136643530
3	15675378	15675379	G	A	66	GENIC	homozygous	136643531
3	15669049	15669080	GGAGGCTGAGTACTAGTAATAGAGTTACGTT		60	GENIC	homozygous	136549647
3	15669428	15669428		TTC	52	GENIC	possibly homozygous	136549648
3	15674429	15674429		AGGG	58	GENIC	homozygous	136549649