chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	105203612	105203613	G	T	9	GENIC	homozygous	125831015
3	105203630	105203631	C	G	10	GENIC	homozygous	125831017
3	105204157	105204158	T	C	7	GENIC	homozygous	111993345
3	105204281	105204282	C	T	11	GENIC	homozygous	111993347
3	105204325	105204326	G	A	8	GENIC	homozygous	111993349
3	105204466	105204467	G	A	14	GENIC	homozygous	111993351
3	105205088	105205089	G	A	20	GENIC	homozygous	111993353
3	105205258	105205259	C	T	12	GENIC	homozygous	111993355
3	105205269	105205270	C	G	13	GENIC	homozygous	111993357
3	105205377	105205378	A	G	13	GENIC	homozygous	111993359
3	105205482	105205483	T	A	20	GENIC	homozygous	111993361
3	105205841	105205842	A	G	8	GENIC	homozygous	111993363
3	105206138	105206139	A	T	12	GENIC	homozygous	111993365
3	105210968	105210969	C	T	14	GENIC	homozygous	111993369
3	105212774	105212775	G	C	26	GENIC	homozygous	125864870
3	105214606	105214607	T	A	9	GENIC	homozygous	111993371