chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90605792	90605793	T	C	11	GENIC	homozygous	114574693
13	90606292	90606293	A	G	9	GENIC	homozygous	114574695
13	90606414	90606415	T	C	7	GENIC	homozygous	114574697
13	90608165	90608166	A	C	16	GENIC	homozygous	114574699
13	90609002	90609003	G	A	15	GENIC	homozygous	114574701
13	90609359	90609360	T	G	14	GENIC	homozygous	114574703
13	90611250	90611251	A	G	14	GENIC	homozygous	114574705
13	90611958	90611959	C	T	9	GENIC	homozygous	114574707
13	90614016	90614017	T	A	6	GENIC	homozygous	114574709
13	90614066	90614067	A	C	8	GENIC	homozygous	114574711
13	90615139	90615140	A	T	20	GENIC	homozygous	114574713
13	90615582	90615583	G	A	9	GENIC	homozygous	114574715
13	90616307	90616308	G	A	15	GENIC	homozygous	114574717
13	90616530	90616531	T	C	8	GENIC	homozygous	114574719
13	90618906	90618907	C	G	3	GENIC	homozygous	114574721
13	90619547	90619548	T	C	8	GENIC	homozygous	114574723
13	90620948	90620949	A	G	11	GENIC	homozygous	114574725
13	90622909	90622910	G	A	12	GENIC	homozygous	114574727
13	90622960	90622961	G	A	9	GENIC	homozygous	114574729
13	90624388	90624389	G	A	14	GENIC	homozygous	114574731
13	90624392	90624393	C	T	14	GENIC	homozygous	114574733
13	90630579	90630580	C	T	13	GENIC	homozygous	114574735
13	90630838	90630839	A	G	11	GENIC	homozygous	114574737
13	90631816	90631817	A	G	12	GENIC	homozygous	114574739
13	90635471	90635472	T	G	12	GENIC	homozygous	114574741
13	90636571	90636572	A	C	3	GENIC	homozygous	114574743
13	90636744	90636745	A	G	10	GENIC	homozygous	114574745
13	90637887	90637888	T	C	6	GENIC	homozygous	114574747
13	90638032	90638033	G	T	11	GENIC	homozygous	114574749
13	90638249	90638250	A	G	7	GENIC	homozygous	114574751
13	90638723	90638724	T	A	11	GENIC	homozygous	114574753
13	90639030	90639031	G	T	15	GENIC	homozygous	114574755
13	90639850	90639851	T	C	8	GENIC	homozygous	114574757
13	90640906	90640907	C	T	7	GENIC	homozygous	114574759
13	90641192	90641193	C	T	13	GENIC	homozygous	114574761