| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127220040-127220219 | Common:2; Rare:41 | ||||
| chr2:127294073-127294219 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387883-127388231 | Common:8; Rare:153 | ||||
| chr2:127526368-127526619 | Common:2; Rare:95 | ||||
| chr2:127526803-127526830 | Rare:8 | ||||
| chr2:127810902-127811349 | Common:2; Rare:132 | ||||
| chr2:127858096-127858219 | Common:2; Rare:66 | ||||
| chr2:127885884-127886538 | Common:2; Rare:180 | ||||
| chr2:128027995-128028235 | Common:1; Rare:76 | ||||
| chr2:128091031-128091354 | Common:8; Rare:105 | ||||
| chr2:130129316-130129718 | Common:6; Rare:122 | ||||
| chr2:130145010-130145162 | Rare:37 | ||||
| chr2:130181528-130181811 | Common:4; Rare:130 | ||||
| chr2:130182185-130182375 | Common:2; Rare:78 | ||||
| chr2:130342043-130342281 | Rare:97; Clinvar:1; Clinvar (pathogenic):1 |