chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	127691089	127691090	T	G	22	INTERGENIC	homozygous	59074678
2	127691557	127691558	G	T	10	INTERGENIC	homozygous	60496933
2	127691560	127691561	G	T	11	INTERGENIC	homozygous	59074679
2	127691665	127691666	G	-	16	INTERGENIC	homozygous	59074680
2	127691668	127691669	G	T	16	INTERGENIC	homozygous	60450115
2	127691694	127691695	G	T	13	INTERGENIC	homozygous	59074681
2	127691696	127691697	G	T	14	INTERGENIC	homozygous	59074682
2	127691710	127691711	G	T	14	INTERGENIC	homozygous	59074683
2	127696726	127696727	G	A	26	INTERGENIC	homozygous	59074694
2	127698430	127698431	G	GA	25	INTERGENIC	homozygous	59074697
2	127698445	127698446	C	T	28	INTERGENIC	homozygous	59074698
2	127698464	127698465	C	-	31	INTERGENIC	homozygous	59074699
2	127701144	127701145	G	T	22	INTERGENIC	homozygous	60891005
2	127701147	127701148	C	T	23	INTERGENIC	homozygous	60891007
2	127701224	127701234	CCGCTTTACT	----------	29	INTERGENIC	homozygous	59074705
2	127701910	127701911	C	CTCTTGGATCA	27	INTERGENIC	homozygous	59074707
2	127702973	127702974	T	G	20	INTERGENIC	homozygous	59074710