| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625842-125625935 | Common:2; Rare:35 | ||||
| chr11:126211641-126211822 | Rare:84 | ||||
| chr11:126268793-126269198 | Common:1; Rare:157; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126303979-126304090 | Rare:65 | ||||
| chr11:126355526-126355771 | Common:2; Rare:69 | ||||
| chr11:128522218-128522546 | Common:1; Rare:98 | ||||
| chr11:128693966-128694201 | Rare:42 | ||||
| chr11:128906017-128906159 | Rare:20 | ||||
| chr11:130314395-130314519 | Common:1; Rare:41 | ||||
| chr11:130448401-130448662 | Rare:64 | ||||
| chr11:131909690-131909930 | Common:1; Rare:40 | ||||
| chr11:131911314-131911492 | Common:1; Rare:68 | ||||
| chr11:131911528-131911606 | Rare:22 | ||||
| chr11:134224533-134224680 | Rare:52 | ||||
| chr11:134253290-134253602 | Common:2; Rare:112; Clinvar (benign):1 |