| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62601592-62602179 | Common:2; Rare:170 | ||||
| chr11:62602301-62602503 | Common:3; Rare:88 | ||||
| chr11:62611833-62612260 | Common:1; Rare:86 | ||||
| chr11:62612361-62612672 | Common:4; Rare:96 | ||||
| chr11:62612740-62612774 | Rare:5 | ||||
| chr11:62621846-62622222 | Common:2; Rare:130 | ||||
| chr11:62646543-62646819 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
| chr11:62653215-62653530 | Common:1; Rare:97 | ||||
| chr11:62653690-62653777 | Rare:6 | ||||
| chr11:62664724-62665013 | Common:2; Rare:95 | ||||
| chr11:62665113-62665594 | Common:7; Rare:226 | ||||
| chr11:62665619-62665724 | Common:1; Rare:24 | ||||
| chr11:62671328-62671391 | Common:2; Rare:22 | ||||
| chr11:62671488-62671921 | Rare:159; Clinvar (benign):1 | ||||
| chr11:62672192-62672416 | Rare:59 |