| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70993467-70994611 | Common:14; Rare:296 | ||||
| chr2:70994691-70995125 | Common:8; Rare:204 | ||||
| chr2:71063901-71064727 | Common:11; Rare:297 | ||||
| chr2:71068031-71068380 | Rare:250 | ||||
| chr2:71068433-71068715 | Rare:344 | ||||
| chr2:71129690-71130070 | Common:1; Rare:173 | ||||
| chr2:71130130-71130797 | Common:20; Rare:494; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:71226994-71227107 | Rare:34 | ||||
| chr2:71276357-71276688 | Rare:308 | ||||
| chr2:71276700-71277040 | Common:3; Rare:123 | ||||
| chr2:71331667-71331936 | Common:6; Rare:130 | ||||
| chr2:71466539-71466742 | Common:5; Rare:48 | ||||
| chr2:72144820-72145330 | Common:4; Rare:229 | ||||
| chr2:72148450-72148820 | Common:4; Rare:81 | ||||
| chr2:72825841-72826078 | Rare:169 |