| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127387225-127387453 | Common:4; Rare:76 | ||||
| chr2:127387897-127388255 | Common:9; Rare:158 | ||||
| chr2:127526422-127526619 | Common:2; Rare:66 | ||||
| chr2:127526803-127526920 | Rare:22 | ||||
| chr2:127811129-127811264 | Rare:42 | ||||
| chr2:127858102-127858215 | Common:1; Rare:58 | ||||
| chr2:127885886-127886526 | Common:2; Rare:177 | ||||
| chr2:128091056-128091369 | Common:8; Rare:101 | ||||
| chr2:130181555-130181797 | Common:3; Rare:105 | ||||
| chr2:130182087-130182336 | Common:2; Rare:96 | ||||
| chr2:130342079-130342281 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:130342642-130342934 | Common:5; Rare:92 | ||||
| chr2:131093378-131093559 | Common:1; Rare:83 | ||||
| chr2:131105194-131105390 | Common:2; Rare:89 | ||||
| chr2:131492749-131492959 | Common:4; Rare:68 |