| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65333659-65333888 | Common:1; Rare:101 | ||||
| chr11:65502885-65503537 | Common:3; Rare:292 | ||||
| chr11:65503550-65504114 | Common:1; Rare:286 | ||||
| chr11:65570038-65570122 | Rare:25 | ||||
| chr11:65570335-65570504 | Rare:69 | ||||
| chr11:65575854-65576122 | Common:3; Rare:81 | ||||
| chr11:65614037-65614151 | Rare:29 | ||||
| chr11:65614186-65614383 | Rare:42 | ||||
| chr11:65662895-65663017 | Common:1; Rare:32 | ||||
| chr11:65860178-65860759 | Common:3; Rare:190 | ||||
| chr11:65888402-65888672 | Common:1; Rare:95 | ||||
| chr11:65890606-65890709 | Common:2; Rare:46 | ||||
| chr11:65919060-65919533 | Rare:170 | ||||
| chr11:65921127-65921418 | Common:1; Rare:87 | ||||
| chr11:66002105-66002374 | Common:3; Rare:82; Clinvar:5; Clinvar (benign):3 |