chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	101060046	101060046		C	14	GENIC	homozygous	127408679
1	101060093	101060094	G	C	14	GENIC	homozygous	108165032
1	101060112	101060112		T	11	GENIC	homozygous	127408680
1	101065570	101065574	CCCC		8	GENIC	homozygous	127408681
1	101065579	101065579		G	5	GENIC	homozygous	127408682
1	101065593	101065594	G		5	GENIC	homozygous	127408683
1	101065606	101065607	G	C	5	GENIC	homozygous	108165033
1	101065631	101065632	T	G	5	GENIC	homozygous	108165034
1	101065654	101065655	T	C	5	GENIC	homozygous	121037123
1	101065656	101065659	TTC		5	GENIC	homozygous	127408684
1	101065660	101065660		TA	5	GENIC	homozygous	127408685
1	101065664	101065665	G	T	4	GENIC	homozygous	121037126
1	101065665	101065666	A	G	4	GENIC	homozygous	121037127
1	101065690	101065691	A		8	GENIC	homozygous	127408686
1	101065695	101065695		T	8	GENIC	homozygous	127408687