chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	16554871	16554872	C	T	31	GENIC	possibly homozygous	119357694
17	16556263	16556264	T	C	19	GENIC	homozygous	119268646
17	16556300	16556301	A	G	29	GENIC	homozygous	119357696
17	16556585	16556586	T	C	20	GENIC	homozygous	119268647
17	16556664	16556665	A	T	25	GENIC	homozygous	110970859
17	16559075	16559076	G	A	28	GENIC	homozygous	110970861
17	16560384	16560385	A	T	22	GENIC	homozygous	111296186
17	16556716	16556717	A	C	20	GENIC	homozygous	111231873
17	16556786	16556787	A	C	41	GENIC	homozygous	111231875
17	16558391	16558392	C	T	27	GENIC	homozygous	111296184
17	16560139	16560140	C	A	30	GENIC	homozygous	111296185
17	16560423	16560424	C	T	23	GENIC	homozygous	111296187
17	16561376	16561377	G	C	21	GENIC	homozygous	110970867
17	16561814	16561815	C	T	19	GENIC	homozygous	110970869
17	16562294	16562295	G	A	25	GENIC	homozygous	111296188
17	16562533	16562534	T	C	28	GENIC	homozygous	110970873
17	16563256	16563257	C	A	16	GENIC	homozygous	110970875
17	16563884	16563885	G	A	12	GENIC	homozygous	111173377
17	16565328	16565329	T	A	7	GENIC	homozygous	119371215
17	16577081	16577082	T	G	14	GENIC	homozygous	111173440
17	16578280	16578281	G	A	25	GENIC	homozygous	110970913
17	16578471	16578472	C	T	27	GENIC	homozygous	111296190