| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219229544-219229891 | Common:2; Rare:110 | ||||
| chr2:219245416-219245511 | Rare:24 | ||||
| chr2:219253884-219254056 | Common:1; Rare:54 | ||||
| chr2:219279203-219279545 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:219498691-219498917 | Common:2; Rare:45 | ||||
| chr2:219543736-219544044 | Common:3; Rare:93 | ||||
| chr2:219597710-219597884 | Common:1; Rare:64 | ||||
| chr2:221572271-221572457 | Common:2; Rare:68 | ||||
| chr2:223957256-223957473 | Common:4; Rare:80 | ||||
| chr2:226835911-226836126 | Common:1; Rare:85 | ||||
| chr2:227164508-227164621 | Rare:25; Clinvar:2 | ||||
| chr2:227325203-227325425 | Common:4; Rare:75 | ||||
| chr2:227717981-227718146 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229921890-229922524 | Common:4; Rare:223 | ||||
| chr2:230068901-230069168 | Common:1; Rare:54 |