| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64778412-64778698 | Common:2; Rare:133 | ||||
| chr11:64778761-64778912 | Common:1; Rare:55 | ||||
| chr11:64803158-64803383 | Rare:88 | ||||
| chr11:64810503-64810821 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65013984-65014252 | Rare:75 | ||||
| chr11:65083980-65084295 | Common:2; Rare:105 | ||||
| chr11:65134480-65134591 | Common:1; Rare:28 | ||||
| chr11:65181289-65181394 | Common:1; Rare:23 | ||||
| chr11:65261759-65262034 | Common:3; Rare:77 | ||||
| chr11:65314738-65314928 | Rare:69 | ||||
| chr11:65333762-65333886 | Common:1; Rare:66 | ||||
| chr11:65386502-65386699 | Rare:64 | ||||
| chr11:65570411-65570510 | Rare:45 | ||||
| chr11:65614216-65614335 | Rare:25 | ||||
| chr11:65615326-65615637 | Common:1; Rare:120 |