| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47186402-47186596 | Rare:47 | ||||
| chr11:47214275-47214529 | Common:1; Rare:28 | ||||
| chr11:47214740-47215137 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47215155-47215311 | Rare:41 | ||||
| chr11:47216313-47216446 | Rare:41 | ||||
| chr11:47248582-47249023 | Common:2; Rare:142; Clinvar (benign):1 | ||||
| chr11:47249128-47249197 | Rare:12 | ||||
| chr11:47268916-47269169 | Rare:42 | ||||
| chr11:47269205-47269837 | Common:4; Rare:180 | ||||
| chr11:47269840-47269920 | Rare:19 | ||||
| chr11:47269927-47270267 | Common:2; Rare:114 | ||||
| chr11:47408100-47408208 | Rare:29 | ||||
| chr11:47408235-47408714 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:47408731-47408770 | Rare:4 | ||||
| chr11:47408859-47408922 | Common:1; Rare:10 |