chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	58952626	58952627	C	A	24	GENIC	homozygous	116788134
10	58952897	58952898	A	G	26	GENIC	homozygous	116607598
10	58953458	58953459	T	C	35	GENIC	homozygous	116607600
10	58954178	58954179	G	A	34	GENIC	homozygous	117011703
10	58954248	58954249	G	A	31	GENIC	homozygous	116607602
10	58954835	58954836	A	G	33	GENIC	homozygous	116607604
10	58956953	58956954	T	A	31	GENIC	homozygous	116788138
10	58957103	58957104	A	G	29	GENIC	homozygous	116788140
10	58957220	58957221	A	G	37	GENIC	homozygous	116788142
10	58957593	58957594	G	A	19	GENIC	homozygous	116788144
10	58958495	58958496	A	G	10	GENIC	homozygous	116607610
10	58958617	58958618	G	T	23	GENIC	homozygous	116788146
10	58958807	58958808	G	A	32	GENIC	homozygous	116788148
10	58964459	58964460	C	T	25	GENIC	homozygous	116788150
10	58967152	58967153	G	A	26	GENIC	homozygous	116788152
10	58968095	58968096	A	G	28	GENIC	homozygous	116788154
10	58968436	58968437	A	G	22	GENIC	homozygous	116607616
10	58969675	58969676	C	T	22	GENIC	homozygous	117011704
10	58970427	58970428	C	T	38	GENIC	homozygous	116788158
10	58971263	58971264	C	T	36	GENIC	homozygous	116788160