| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387151-20387845 | Common:11; Rare:207 | ||||
| chr11:20387951-20388113 | Common:1; Rare:66 | ||||
| chr11:20388124-20388304 | Rare:59 | ||||
| chr11:22625091-22625681 | Common:5; Rare:254; Clinvar:21; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr11:22625729-22626213 | Common:4; Rare:141; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:22626293-22626567 | Common:1; Rare:40 | ||||
| chr11:22829300-22829434 | Common:1; Rare:32 | ||||
| chr11:22829714-22830055 | Common:4; Rare:126 | ||||
| chr11:26993966-26994334 | Common:1; Rare:80 | ||||
| chr11:27040516-27040723 | Rare:40 | ||||
| chr11:27363066-27363454 | Rare:163 | ||||
| chr11:27385390-27385496 | Rare:26 | ||||
| chr11:27471767-27472322 | Common:4; Rare:140 | ||||
| chr11:27472464-27472648 | Common:1; Rare:51 | ||||
| chr11:27472673-27472976 | Common:1; Rare:71 |