chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	58043979	58043980	G	T	25	GENIC	homozygous	113816734
5	58046076	58046077	C	T	25	GENIC	homozygous	113816740
5	58051178	58051179	A	G	17	GENIC	homozygous	113816742
5	58052089	58052090	G	A	33	GENIC	homozygous	113816744
5	58053094	58053095	G	A	20	GENIC	homozygous	113816748
5	58055825	58055826	A	G	4	GENIC	homozygous	113816750
5	58056904	58056905	A	G	27	GENIC	homozygous	113816752
5	58059510	58059511	A	T	32	GENIC	homozygous	113816756
5	58060151	58060152	T	C	20	GENIC	homozygous	113816758
5	58060621	58060622	G	A	13	GENIC	homozygous	113816760
5	58065408	58065409	A	C	36	GENIC	homozygous	113816764
5	58066712	58066713	A	G	29	GENIC	homozygous	118853852
5	58071716	58071717	A	G	23	GENIC	homozygous	113816772
5	58072358	58072359	G	T	34	GENIC	homozygous	113816774
5	58073397	58073398	G	T	25	GENIC	homozygous	113816778
5	58073407	58073408	G	T	21	GENIC	homozygous	118842937
5	58073646	58073647	A	G	39	GENIC	homozygous	113816780
5	58074953	58074954	G	A	18	GENIC	homozygous	113816782
5	58075694	58075695	C	G	26	GENIC	homozygous	113816784
5	58076171	58076172	G	A	36	GENIC	homozygous	113816786
5	58076196	58076197	T	C	35	GENIC	homozygous	113816788
5	58076529	58076530	C	T	24	GENIC	homozygous	113816790
5	58076581	58076582	A	G	34	GENIC	homozygous	113816792