| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178482477-178482607 | Common:1; Rare:25 | ||||
| chr2:178523030-178523307 | Rare:84 | ||||
| chr2:178530812-178530987 | Common:4; Rare:41; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:178820190-178820270 | Common:2; Rare:17 | ||||
| chr2:179021256-179021439 | Common:1; Rare:25 | ||||
| chr2:179024539-179024599 | Rare:10 | ||||
| chr2:179024603-179024661 | Common:1; Rare:13 | ||||
| chr2:179031802-179032260 | Common:1; Rare:93 | ||||
| chr2:179049161-179049259 | Rare:18 | ||||
| chr2:179049326-179049480 | Common:1; Rare:35 | ||||
| chr2:179096109-179096272 | Rare:36 | ||||
| chr2:179995822-179996006 | Rare:21 | ||||
| chr2:181123843-181124038 | Common:1; Rare:32 | ||||
| chr2:181124701-181124774 | Common:1; Rare:13 | ||||
| chr2:181165293-181165435 | Rare:28 |