| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46593991-46594133 | Common:2; Rare:31 | ||||
| chr11:46617239-46617585 | Common:5; Rare:96 | ||||
| chr11:46700965-46701086 | Common:1; Rare:44 | ||||
| chr11:46846140-46846412 | Common:1; Rare:85 | ||||
| chr11:47186398-47186529 | Rare:38 | ||||
| chr11:47214843-47215003 | Common:1; Rare:42 | ||||
| chr11:47248781-47248938 | Rare:63 | ||||
| chr11:47269074-47269385 | Common:1; Rare:63 | ||||
| chr11:47269550-47269714 | Common:1; Rare:56 | ||||
| chr11:47269981-47270236 | Common:2; Rare:89 | ||||
| chr11:47426416-47426648 | Rare:55 | ||||
| chr11:47565499-47565650 | Common:3; Rare:30 | ||||
| chr11:47578967-47579106 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642443-47642805 | Rare:132 | ||||
| chr11:47848321-47848438 | Rare:59 |