chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	33109134	33109135	C	T	56	GENIC	homozygous	113417757
14	33110077	33110078	A	G	47	GENIC	homozygous	113417758
14	33110427	33110428	A	G	61	GENIC	homozygous	113417759
14	33112092	33112093	A	C	47	GENIC	homozygous	113417760
14	33112159	33112160	C	A	39	GENIC	homozygous	113417761
14	33113133	33113134	T	A	45	GENIC	homozygous	113417762
14	33113534	33113534		T	44	GENIC	homozygous	129143592
14	33114054	33114055	C	A	40	GENIC	homozygous	113417763
14	33114197	33114198	T	C	38	GENIC	homozygous	113978541
14	33114200	33114200		A	39	GENIC	homozygous	129143593
14	33114303	33114303		G	32	GENIC	homozygous	129143594
14	33114313	33114314	G	T	30	GENIC	homozygous	113417764
14	33114351	33114352	T	C	31	GENIC	homozygous	113417765
14	33114906	33114907	T	C	49	GENIC	homozygous	113417766
14	33115484	33115485	A	G	35	GENIC	homozygous	113417767
14	33117392	33117393	G	A	44	GENIC	homozygous	113417768
14	33120545	33120546	T	C	35	GENIC	homozygous	113417769
14	33120690	33120691	A	G	31	GENIC	homozygous	113417770
14	33122763	33122763		TTG	37	GENIC	possibly homozygous	129143595
14	33122826	33122827	T	C	45	GENIC	homozygous	113417771
14	33122838	33122839	T	C	44	GENIC	homozygous	113417772
14	33123033	33123034	A	G	44	GENIC	homozygous	113786900
14	33123420	33123421	T	C	37	GENIC	homozygous	113417773
14	33123451	33123451		CG	33	GENIC	homozygous	129143596
14	33123706	33123707	T	C	39	GENIC	homozygous	113417774
14	33123775	33123776	G	A	41	GENIC	homozygous	113417775
14	33123833	33123834	G	A	47	GENIC	homozygous	113417776
14	33123977	33123978	A	G	37	GENIC	homozygous	113417777
14	33124045	33124046	G	A	29	GENIC	homozygous	113417778
14	33116592	33116593	A	C	29	GENIC	homozygous	113672234
14	33122785	33122786	A	G	43	GENIC	possibly homozygous	113672236
14	33116649	33116650	G	T	20	GENIC	homozygous	118687414
14	33123004	33123005	C	T	45	GENIC	homozygous	113584880