chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	60570959	60570960	T	G	31	GENIC	homozygous	114365681
13	60571699	60571700	C	T	31	GENIC	homozygous	114365682
13	60573042	60573043	C	T	32	GENIC	homozygous	114365683
13	60574966	60574967	A	G	31	GENIC	homozygous	114365684
13	60575615	60575616	G	A	27	GENIC	homozygous	114625089
13	60578261	60578262	G	A	18	GENIC	homozygous	114365686
13	60578285	60578286	T	C	20	GENIC	homozygous	114625091
13	60578549	60578550	G	C	27	GENIC	homozygous	114365687
13	60578813	60578814	T	C	16	GENIC	homozygous	114365688
13	60579280	60579281	C	T	10	GENIC	homozygous	114722884
13	60580043	60580044	T	A	25	GENIC	homozygous	114365689
13	60581009	60581010	A	G	30	GENIC	homozygous	114365690
13	60585103	60585104	T	C	25	GENIC	homozygous	114365691
13	60586849	60586850	A	G	16	GENIC	homozygous	114625093
13	60588355	60588356	T	C	19	GENIC	homozygous	114365692
13	60589054	60589055	G	T	14	GENIC	homozygous	114625097
13	60590731	60590732	A	G	17	GENIC	homozygous	114365695
13	60591979	60591980	C	T	22	GENIC	homozygous	114625099
13	60592437	60592438	A	T	30	GENIC	homozygous	114678458
13	60592470	60592471	G	T	27	GENIC	homozygous	114678460
13	60592474	60592475	G	T	29	GENIC	possibly homozygous	114678462
13	60592478	60592479	G	T	28	GENIC	possibly homozygous	114678464
13	60592707	60592708	T	C	26	GENIC	homozygous	114365699
13	60592854	60592855	C	T	19	GENIC	homozygous	114365700
13	60593156	60593157	C	T	19	GENIC	homozygous	114365701
13	60595019	60595020	T	G	23	GENIC	homozygous	114365703
13	60596111	60596112	T	A	16	GENIC	homozygous	114365704
13	60596476	60596477	A	C	18	GENIC	homozygous	114365705
13	60598979	60598980	A	G	25	GENIC	homozygous	114365706
13	60600446	60600447	C	T	24	GENIC	homozygous	114365707
13	60600560	60600561	A	G	30	GENIC	homozygous	114365709
13	60601058	60601059	T	C	21	GENIC	homozygous	114365712
13	60601164	60601165	A	G	23	GENIC	homozygous	114365713
13	60601888	60601889	G	C	29	GENIC	homozygous	114365714