chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90186343	90186344	C	T	23	GENIC	homozygous	114573893
13	90190285	90190286	T	C	16	GENIC	homozygous	114573895
13	90192751	90192752	T	A	24	GENIC	homozygous	114573897
13	90192760	90192761	A	T	22	GENIC	homozygous	114573899
13	90192814	90192815	A	C	17	GENIC	homozygous	114573901
13	90192908	90192909	T	G	16	GENIC	homozygous	114573903
13	90195859	90195860	G	A	13	GENIC	homozygous	114693367
13	90196775	90196776	G	A	19	GENIC	homozygous	114573904
13	90198629	90198630	A	G	37	GENIC	homozygous	114573906
13	90199353	90199354	A	G	16	GENIC	homozygous	114573908
13	90200317	90200318	G	A	23	GENIC	possibly homozygous	114573910
13	90201240	90201241	A	G	14	GENIC	homozygous	114573912
13	90203074	90203075	A	T	23	GENIC	homozygous	114573914
13	90203206	90203207	A	G	26	GENIC	homozygous	114573916
13	90203299	90203300	T	A	16	GENIC	homozygous	114573917
13	90204064	90204065	T	C	19	GENIC	homozygous	114573919
13	90205298	90205299	T	C	20	GENIC	homozygous	114573920
13	90205799	90205800	G	A	19	GENIC	homozygous	114573922
13	90208928	90208929	A	G	9	GENIC	homozygous	114573924
13	90209805	90209806	T	C	16	GENIC	homozygous	114573925
13	90211243	90211244	G	T	25	GENIC	homozygous	114573927
13	90211244	90211245	T	G	26	GENIC	homozygous	114573928
13	90212383	90212384	C	T	19	GENIC	homozygous	114858755
13	90214280	90214281	G	A	13	GENIC	homozygous	114573934
13	90214737	90214738	C	A	14	GENIC	heterozygous	114858757
13	90216356	90216357	G	C	17	GENIC	homozygous	114573936
13	90218149	90218150	T	C	23	GENIC	homozygous	114573938
13	90218441	90218442	A	G	17	GENIC	homozygous	114573940
13	90218633	90218634	A	T	24	GENIC	homozygous	114693369
13	90218679	90218680	C	G	19	GENIC	homozygous	114573941
13	90219099	90219100	T	C	32	GENIC	homozygous	114573943