| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:695598-695646 | Common:1; Rare:12 | ||||
| chr11:695724-695826 | Rare:34 | ||||
| chr11:706013-706267 | Common:2; Rare:80 | ||||
| chr11:707066-707083 | Rare:3 | ||||
| chr11:721088-721340 | Rare:112 | ||||
| chr11:747303-747569 | Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:755731-755889 | Rare:43 | ||||
| chr11:764008-764430 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:764671-764837 | Common:1; Rare:59; Clinvar:1 | ||||
| chr11:777452-777638 | Common:1; Rare:85 | ||||
| chr11:798262-798374 | Rare:32 | ||||
| chr11:809495-809647 | Common:2; Rare:40 | ||||
| chr11:809799-810038 | Common:2; Rare:110 | ||||
| chr11:826131-826182 | Rare:10 | ||||
| chr11:827098-827322 | Common:2; Rare:58 |