| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108009230-108009294 | Rare:24 | ||||
| chr11:108009295-108009369 | Rare:34 | ||||
| chr11:108133596-108133937 | Rare:78; Clinvar (pathogenic):2 | ||||
| chr11:108222573-108223128 | Common:1; Rare:179; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223272-108223367 | Rare:31 | ||||
| chr11:108467479-108467618 | Common:3; Rare:55 | ||||
| chr11:111299649-111299773 | Common:2; Rare:31 | ||||
| chr11:111766332-111766463 | Common:1; Rare:82 | ||||
| chr11:111878721-111879011 | Common:2; Rare:91 | ||||
| chr11:111879147-111879562 | Common:1; Rare:131 | ||||
| chr11:111912611-111912765 | Common:1; Rare:36 | ||||
| chr11:111913131-111913281 | Rare:43 | ||||
| chr11:111923722-111923806 | Common:1; Rare:9 | ||||
| chr11:112025301-112025456 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:112073987-112074358 | Common:1; Rare:79 |