chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	124125159	124125161	TC		45	GENIC	homozygous	137710223
6	124125192	124125193	A	G	45	GENIC	homozygous	137908351
6	124125203	124125204	C	T	45	GENIC	homozygous	137908352
6	124125313	124125314	T	A	49	GENIC	homozygous	137908353
6	124125401	124125401		AATGGAGCT	37	GENIC	homozygous	137710224
6	124125417	124125418	C	T	49	GENIC	homozygous	137908354
6	124125488	124125489	G	A	49	GENIC	homozygous	137908355
6	124125512	124125513	C	T	51	GENIC	homozygous	137908356
6	124125562	124125563	A	G	52	GENIC	homozygous	137908357
6	124125644	124125644		A	47	GENIC	possibly homozygous	137710225
6	124125838	124125839	C	A	52	GENIC	homozygous	137908358
6	124125852	124125853	G	T	54	GENIC	homozygous	137908359
6	124126047	124126053	GCCTGG		50	GENIC	homozygous	137710226
6	124126121	124126123	GT		46	GENIC	homozygous	137710227
6	124126547	124126548	G	A	54	GENIC	homozygous	137908360
6	124126734	124126735	A	G	49	GENIC	homozygous	137908361
6	124127219	124127220	A	G	71	GENIC	homozygous	137908362
6	124127522	124127523	C	T	54	GENIC	homozygous	137908363
6	124128220	124128221	T	C	47	GENIC	homozygous	137908364
6	124130116	124130117	A	G	64	GENIC	homozygous	137908365