chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17028310	17028311	C	A	23	GENIC	homozygous	142431501
14	17028610	17028611	T	C	46	GENIC	homozygous	139462033
14	17028853	17028854	C	T	59	GENIC	homozygous	142431502
14	17029016	17029042	TATATGTGTGTGTGTGTGTGTATTTA		46	GENIC	homozygous	139381804
14	17029159	17029160	T	C	43	GENIC	homozygous	142431503
14	17029551	17029552	A	G	59	GENIC	homozygous	142431504
14	17029580	17029581	T	C	54	GENIC	homozygous	142431505
14	17030296	17030297	A	G	17	GENIC	homozygous	142431506
14	17030298	17030299	A	G	17	GENIC	homozygous	142431507
14	17034372	17034373	C	T	63	GENIC	homozygous	142431508
14	17034991	17034991		CT	53	GENIC	homozygous	139381808
14	17035995	17035996	C	A	64	GENIC	possibly homozygous	142431509
14	17037014	17037015	A	T	65	GENIC	homozygous	142431510
14	17037270	17037271	A	G	57	GENIC	homozygous	142431511
14	17037514	17037515	T	A	66	GENIC	homozygous	142431512
14	17038139	17038140	T	C	63	GENIC	homozygous	139462041
14	17038302	17038303	C	T	61	GENIC	homozygous	142431513
14	17038350	17038351	T	C	48	GENIC	homozygous	142431514
14	17038688	17038689	C	G	55	GENIC	homozygous	142431515
14	17038720	17038721	C	T	51	GENIC	homozygous	142431516
14	17038737	17038738	T	C	52	GENIC	homozygous	142431517
14	17038806	17038807	C	A	44	GENIC	homozygous	142431518
14	17040517	17040518	C	A	57	GENIC	homozygous	142431522
14	17038900	17038901	T	C	44	GENIC	homozygous	139462042
14	17039029	17039030	C	T	46	GENIC	homozygous	142431519
14	17039625	17039626	A	G	51	GENIC	possibly homozygous	142431520
14	17040175	17040176	G	A	53	GENIC	homozygous	142431521
14	17030289	17030291	TC		10	GENIC	heterozygous	142418858
14	17040613	17040614	C	A	49	GENIC	homozygous	142431523