chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	14370133	14370134	T	C	52	GENIC	heterozygous	119266110
17	14370183	14370184	T	G	66	GENIC	heterozygous	119266111
17	14370221	14370222	C	T	64	GENIC	heterozygous	119266112
17	14370224	14370225	G	A	64	GENIC	heterozygous	119266113
17	14370581	14370582	T	C	30	GENIC	homozygous	119266115
17	14370990	14370991	G	T	32	GENIC	heterozygous	119266116
17	14371018	14371019	G	A	37	GENIC	heterozygous	119266117
17	14371025	14371026	C	A	18	GENIC	homozygous	119266118
17	14371026	14371027	T	G	18	GENIC	homozygous	119266119
17	14371029	14371030	C	T	36	GENIC	heterozygous	119266120
17	14371050	14371051	G	A	39	GENIC	heterozygous	119266121
17	14371156	14371157	C	T	48	GENIC	heterozygous	119266124
17	14371166	14371167	C	T	53	GENIC	heterozygous	119266125
17	14371180	14371181	C	A	64	GENIC	heterozygous	119266126
17	14371199	14371200	C	T	65	GENIC	heterozygous	119266127
17	14371205	14371206	G	A	63	GENIC	heterozygous	119266128
17	14371218	14371219	C	T	72	GENIC	heterozygous	119266129
17	14371255	14371256	T	C	79	GENIC	heterozygous	119266130
17	14371280	14371281	G	T	71	GENIC	heterozygous	119266131
17	14371325	14371326	T	C	67	GENIC	heterozygous	119266132