chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	124051544	124051545	T	C	8	GENIC	homozygous	119407895
4	124051913	124051914	C	A	11	GENIC	homozygous	113380725
4	124054209	124054210	A	G	7	GENIC	homozygous	113380733
4	124057305	124057306	T	G	10	GENIC	homozygous	113380741
4	124058214	124058215	A	G	5	GENIC	homozygous	113380745
4	124059808	124059809	G	C	5	GENIC	homozygous	119407899
4	124053389	124053390	A	G	6	GENIC	homozygous	119407896
4	124053657	124053658	T	G	9	GENIC	homozygous	119407897
4	124058795	124058796	C	T	4	GENIC	homozygous	119407898
4	124060835	124060836	G	A	4	GENIC	homozygous	113380747
4	124061788	124061789	A	G	4	GENIC	homozygous	113380749
4	124063070	124063071	A	G	4	GENIC	homozygous	113380751
4	124064571	124064572	C	T	5	GENIC	homozygous	119407900
4	124067387	124067388	C	T	6	GENIC	homozygous	113380755
4	124067611	124067612	A	G	6	GENIC	homozygous	113380757
4	124070670	124070671	T	C	5	GENIC	homozygous	113380759
4	124070712	124070713	A	G	6	GENIC	homozygous	113380761
4	124070943	124070944	C	A	4	GENIC	homozygous	119535071
4	124077971	124077972	G	A	3	GENIC	homozygous	119407901
4	124078006	124078007	G	A	6	GENIC	homozygous	119407902
4	124079918	124079919	A	C	8	GENIC	homozygous	119407903