| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181525-130181787 | Common:7; Rare:229 | ||||
| chr2:130182072-130182400 | Common:3; Rare:195 | ||||
| chr2:130342093-130342285 | Rare:131; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr2:130342641-130342952 | Common:11; Rare:202 | ||||
| chr2:130355913-130356121 | Common:2; Rare:59 | ||||
| chr2:131092820-131093300 | Common:2; Rare:209 | ||||
| chr2:131093357-131093594 | Common:2; Rare:210 | ||||
| chr2:131105192-131105399 | Common:4; Rare:178 | ||||
| chr2:131492226-131492499 | Common:5; Rare:151 | ||||
| chr2:131492686-131493125 | Common:12; Rare:205 | ||||
| chr2:132416412-132416858 | Common:4; Rare:229 | ||||
| chr2:134119788-134120231 | Common:5; Rare:282 | ||||
| chr2:134918589-134918914 | Common:2; Rare:242 | ||||
| chr2:134919040-134919690 | Common:11; Rare:268 | ||||
| chr2:135530699-135531060 | Common:7; Rare:142 |