chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104138095	104138096	T	C	19	GENIC	homozygous	116834902
10	104139936	104139937	A	G	20	GENIC	homozygous	117030804
10	104141631	104141632	T	C	17	GENIC	homozygous	116834904
10	104141726	104141727	G	A	17	GENIC	homozygous	117030806
10	104143864	104143865	T	C	16	GENIC	homozygous	116834908
10	104143910	104143911	G	A	10	GENIC	homozygous	117030808
10	104145114	104145115	A	G	23	GENIC	homozygous	116834910
10	104149429	104149430	T	C	18	GENIC	homozygous	116713724
10	104149431	104149432	T	C	18	GENIC	homozygous	116713726
10	104149459	104149460	T	C	17	GENIC	homozygous	116834912
10	104153190	104153191	G	A	34	GENIC	homozygous	116834914
10	104153424	104153425	G	A	25	GENIC	homozygous	116834916
10	104153952	104153953	C	T	21	GENIC	homozygous	116834918