| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181481-130181815 | Common:12; Rare:408 | ||||
| chr2:130182018-130182561 | Common:6; Rare:396 | ||||
| chr2:130341026-130341742 | Rare:202 | ||||
| chr2:130342024-130342324 | Rare:265; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr2:130342563-130342984 | Common:20; Rare:349 | ||||
| chr2:130355844-130356301 | Common:18; Rare:306 | ||||
| chr2:130356409-130356570 | Common:5; Rare:55 | ||||
| chr2:130371790-130372280 | Common:6; Rare:144 | ||||
| chr2:130372503-130372795 | Common:3; Rare:218 | ||||
| chr2:130836749-130837012 | Common:6; Rare:247 | ||||
| chr2:131093066-131093184 | Rare:65 | ||||
| chr2:131093131-131093255 | Common:1; Rare:42 | ||||
| chr2:131093300-131093856 | Common:4; Rare:447 | ||||
| chr2:131104780-131105422 | Common:11; Rare:406 | ||||
| chr2:131491968-131492499 | Common:13; Rare:332 |