| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73598071-73598353 | Common:2; Rare:79 | ||||
| chr11:73598473-73598679 | Common:9; Rare:54 | ||||
| chr11:73647370-73647720 | Common:1; Rare:65 | ||||
| chr11:73652309-73652767 | Common:7; Rare:148 | ||||
| chr11:73761027-73761444 | Common:4; Rare:111 | ||||
| chr11:73787055-73787562 | Common:3; Rare:147 | ||||
| chr11:73787746-73788310 | Common:8; Rare:148 | ||||
| chr11:73876627-73877108 | Common:6; Rare:148 | ||||
| chr11:73982759-73983125 | Common:7; Rare:107 | ||||
| chr11:73983176-73983443 | Common:3; Rare:70 | ||||
| chr11:74170933-74171421 | Common:3; Rare:161 | ||||
| chr11:74398374-74398556 | Common:3; Rare:42 | ||||
| chr11:74398630-74398960 | Rare:95 | ||||
| chr11:74493215-74493433 | Common:1; Rare:99; Clinvar (pathogenic):1 | ||||
| chr11:74493667-74493858 | Common:1; Rare:75 |