chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	147504996	147504997	T	C	43	GENIC	homozygous	119997421
3	147506297	147506298	C	G	42	GENIC	homozygous	119997423
3	147506343	147506344	G	A	33	GENIC	possibly homozygous	119997425
3	147508769	147508770	C	T	52	GENIC	homozygous	119997427
3	147509758	147509758		T	6	GENIC	heterozygous	129892170
3	147510312	147510313	G	A	56	GENIC	homozygous	119997429
3	147510620	147510621	T	C	92	GENIC	homozygous	119997431
3	147511256	147511257	C	T	53	GENIC	homozygous	119997433
3	147511512	147511513	A	G	62	GENIC	homozygous	119997435
3	147512369	147512370	G	A	52	GENIC	homozygous	119997437
3	147514452	147514453	A	T	55	GENIC	homozygous	119997439
3	147514816	147514817	T	C	41	GENIC	homozygous	119997441
3	147515392	147515393	C	T	54	GENIC	homozygous	119997443
3	147515663	147515664	C	T	52	GENIC	homozygous	119997445
3	147516810	147516811	T	C	43	GENIC	possibly homozygous	119997447
3	147516941	147516942	C	T	51	GENIC	homozygous	119997449
3	147517435	147517436	C	T	39	GENIC	homozygous	119997451
3	147517450	147517451	G	A	36	GENIC	homozygous	119997453
3	147516362	147516363	T	C	38	GENIC	homozygous	120102609
3	147512289	147512309	CCTTCTTCCTTCCTTCCTTC		33	GENIC	homozygous	131329840
3	147512338	147512339	T	A	47	GENIC	homozygous	120102607