chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	58043979	58043980	G	T	32	GENIC	homozygous	113816734
5	58044490	58044491	T	C	43	GENIC	homozygous	113816736
5	58045610	58045611	G	A	32	GENIC	homozygous	113816738
5	58046076	58046077	C	T	47	GENIC	homozygous	113816740
5	58051178	58051179	A	G	57	GENIC	homozygous	113816742
5	58052089	58052090	G	A	40	GENIC	homozygous	113816744
5	58052256	58052257	C	T	55	GENIC	homozygous	113816746
5	58053094	58053095	G	A	30	GENIC	homozygous	113816748
5	58056904	58056905	A	G	40	GENIC	homozygous	113816752
5	58057464	58057465	C	A	37	GENIC	homozygous	113816754
5	58059510	58059511	A	T	32	GENIC	possibly homozygous	113816756
5	58060151	58060152	T	C	35	GENIC	homozygous	113816758
5	58060621	58060622	G	A	27	GENIC	homozygous	113816760
5	58061604	58061605	C	G	50	GENIC	heterozygous	113816762
5	58065408	58065409	A	C	59	GENIC	homozygous	113816764
5	58066939	58066940	G	A	25	GENIC	possibly homozygous	113816766
5	58067054	58067055	A	G	14	GENIC	homozygous	113816768
5	58067661	58067662	A	C	5	GENIC	homozygous	113816770
5	58071716	58071717	A	G	30	GENIC	homozygous	113816772
5	58072358	58072359	G	T	35	GENIC	homozygous	113816774
5	58072606	58072607	G	T	11	GENIC	homozygous	113816776
5	58073397	58073398	G	T	34	GENIC	homozygous	113816778
5	58073646	58073647	A	G	42	GENIC	homozygous	113816780
5	58074953	58074954	G	A	34	GENIC	homozygous	113816782
5	58075694	58075695	C	G	31	GENIC	homozygous	113816784
5	58076171	58076172	G	A	32	GENIC	homozygous	113816786
5	58076196	58076197	T	C	36	GENIC	homozygous	113816788
5	58076529	58076530	C	T	31	GENIC	homozygous	113816790
5	58076581	58076582	A	G	25	GENIC	homozygous	113816792
5	58076755	58076756	C	T	11	GENIC	homozygous	113816794
5	58076806	58076807	G	T	25	GENIC	homozygous	113816796
5	58077461	58077462	T	G	11	GENIC	homozygous	113816798
5	58077545	58077546	C	T	10	GENIC	homozygous	113816800
5	58077586	58077587	A	C	6	GENIC	homozygous	113816802