| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62601225-62601346 | Rare:65 | ||||
| chr11:62601420-62601588 | Common:1; Rare:47 | ||||
| chr11:62601605-62602181 | Common:2; Rare:266 | ||||
| chr11:62611430-62611930 | Rare:221 | ||||
| chr11:62612463-62612644 | Common:4; Rare:105 | ||||
| chr11:62612722-62612877 | Common:1; Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
| chr11:62621881-62622236 | Common:4; Rare:219 | ||||
| chr11:62646559-62646810 | Common:2; Rare:166; Clinvar (pathogenic):1 | ||||
| chr11:62653095-62653850 | Common:14; Rare:234 | ||||
| chr11:62665143-62665360 | Common:9; Rare:194 | ||||
| chr11:62671744-62671992 | Common:2; Rare:183; Clinvar (benign):2 | ||||
| chr11:62678820-62679201 | Rare:229 | ||||
| chr11:62706214-62706445 | Common:6; Rare:179; Clinvar (benign):10 | ||||
| chr11:62726755-62727316 | Common:5; Rare:302 | ||||
| chr11:62727314-62727740 | Common:1; Rare:306 |