chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	124125192	124125193	A	G	50	GENIC	homozygous	137908351
6	124125203	124125204	C	T	48	GENIC	homozygous	137908352
6	124125301	124125302	C	T	39	GENIC	homozygous	143990748
6	124125313	124125314	T	A	40	GENIC	homozygous	137908353
6	124125401	124125401		AATGGAGCT	43	GENIC	homozygous	137710224
6	124125417	124125418	C	T	55	GENIC	homozygous	137908354
6	124125488	124125489	G	A	67	GENIC	homozygous	137908355
6	124125562	124125563	A	G	57	GENIC	homozygous	137908357
6	124125852	124125853	G	T	56	GENIC	possibly homozygous	137908359
6	124126121	124126123	GT		49	GENIC	homozygous	137710227
6	124126547	124126548	G	A	49	GENIC	homozygous	137908360
6	124126734	124126735	A	G	57	GENIC	homozygous	137908361
6	124127219	124127220	A	G	45	GENIC	homozygous	137908362
6	124127248	124127249	A	T	44	GENIC	homozygous	143990749
6	124127562	124127563	T	C	60	GENIC	homozygous	143990750
6	124127571	124127572	T	C	57	GENIC	homozygous	143990751
6	124127799	124127800	A	C	46	GENIC	homozygous	143990752
6	124127959	124127959		CCCCCCA	9	GENIC	possibly homozygous	147263844
6	124128220	124128221	T	C	46	GENIC	homozygous	137908364
6	124130512	124130513	C	T	67	GENIC	homozygous	143990753