chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	49837919	49837920	A	G	45	GENIC	possibly homozygous	117868390
9	49837998	49837999	C	A	38	GENIC	homozygous	117868391
9	49838206	49838207	G	A	41	GENIC	homozygous	117868392
9	49838323	49838324	A	G	42	GENIC	homozygous	117868393
9	49838473	49838474	C	T	26	GENIC	homozygous	117868394
9	49838497	49838498	T	C	27	GENIC	homozygous	117868395
9	49838842	49838843	T	C	42	GENIC	homozygous	117868396
9	49839100	49839101	A	G	44	GENIC	homozygous	117868397
9	49839148	49839149	C	T	39	GENIC	homozygous	117868398
9	49839609	49839610	T	C	40	GENIC	homozygous	117868399
9	49839626	49839627	A	T	42	GENIC	homozygous	117868400
9	49839694	49839695	A	G	37	GENIC	homozygous	117868401
9	49839808	49839809	G	T	36	GENIC	homozygous	117868402
9	49840237	49840238	G	A	34	GENIC	homozygous	117868403
9	49840670	49840671	T	G	22	GENIC	homozygous	117868404
9	49840704	49840705	G	C	21	GENIC	homozygous	117868405
9	49840777	49840778	A	T	29	GENIC	homozygous	117868406
9	49840981	49840982	A	G	35	GENIC	homozygous	117868407
9	49841053	49841054	G	C	34	GENIC	homozygous	117868408
9	49841076	49841077	A	G	36	GENIC	homozygous	117868409
9	49841092	49841093	G	A	38	GENIC	homozygous	117868410
9	49841119	49841120	T	C	39	GENIC	homozygous	117868411
9	49841160	49841161	A	G	45	GENIC	homozygous	117868412
9	49841232	49841233	A	C	29	GENIC	homozygous	117868413