chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10002582	10002582		TTTC	29	GENIC	heterozygous	144171969
17	10003740	10003741	A	G	44	GENIC	homozygous	140052086
17	10006585	10006586	A	G	53	GENIC	homozygous	140052087
17	10006909	10006910	T	C	60	GENIC	homozygous	140052088
17	10007222	10007223	T	C	68	GENIC	homozygous	140052089
17	10007570	10007571	C	T	56	GENIC	homozygous	140052090
17	10007767	10007768	A	G	46	GENIC	homozygous	140052091
17	10007932	10007933	C	G	65	GENIC	homozygous	140052092
17	10008714	10008715	T	C	48	GENIC	homozygous	140052093
17	10009179	10009180	A	C	43	GENIC	homozygous	140052094
17	10009187	10009188	A	C	45	GENIC	homozygous	140052095
17	10009237	10009238	A	G	46	GENIC	homozygous	140052096
17	10010031	10010032	C	T	48	GENIC	homozygous	140052097
17	10010995	10010996	A	G	41	GENIC	homozygous	140052098
17	10011130	10011131	T	C	42	GENIC	homozygous	140052099
17	10011658	10011659	G	A	66	GENIC	homozygous	140052100
17	10009150	10009164	CGAAAAAAAAAAAA		38	GENIC	homozygous	140008743
17	10014643	10014647	TCCC		22	GENIC	heterozygous	140008744