chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	100971373	100971374	A	G	39	GENIC	homozygous	109563291
1	100971520	100971521	T	C	32	GENIC	homozygous	109563292
1	100973115	100973116	A	G	29	GENIC	homozygous	109563293
1	100973291	100973292	T	C	18	GENIC	homozygous	109563294
1	100974489	100974490	C	G	32	GENIC	homozygous	109563295
1	100975189	100975190	C	T	36	GENIC	homozygous	109563296
1	100975327	100975328	C	T	38	GENIC	homozygous	109563297
1	100975532	100975533	T	C	34	GENIC	homozygous	109563298
1	100976093	100976094	A	G	25	GENIC	homozygous	109563299
1	100976709	100976710	A	G	38	GENIC	homozygous	109563301
1	100977276	100977277	G	T	20	GENIC	homozygous	109563302
1	100977446	100977447	C	T	34	GENIC	homozygous	109563303
1	100978038	100978039	G	A	37	GENIC	homozygous	109563304
1	100979171	100979172	A	G	28	GENIC	homozygous	109563305
1	100979911	100979912	T	A	23	GENIC	homozygous	109563306