| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214832-47215127 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248765-47248955 | Rare:79 | ||||
| chr11:47257768-47258062 | Rare:51 | ||||
| chr11:47269083-47269409 | Common:1; Rare:68 | ||||
| chr11:47269525-47269727 | Common:1; Rare:69 | ||||
| chr11:47269972-47270217 | Common:1; Rare:88 | ||||
| chr11:47553048-47553281 | Common:2; Rare:91 | ||||
| chr11:47565478-47565643 | Common:3; Rare:32 | ||||
| chr11:47578920-47579094 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47582169-47582428 | Rare:81; Clinvar:1 | ||||
| chr11:47642447-47642805 | Rare:130 | ||||
| chr11:47767109-47767432 | Common:6; Rare:139 | ||||
| chr11:47848317-47848406 | Rare:47 | ||||
| chr11:47848511-47848683 | Common:3; Rare:38 | ||||
| chr11:48044127-48044368 | Rare:38 |