| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:84166967-84167058 | Common:1; Rare:28 | ||||
| chr11:84437547-84437733 | Rare:42 | ||||
| chr11:85627244-85627388 | Rare:28 | ||||
| chr11:85627794-85627858 | Rare:9 | ||||
| chr11:85628317-85628664 | Common:7; Rare:121 | ||||
| chr11:85647882-85648036 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:85663273-85663485 | Rare:30 | ||||
| chr11:85663871-85663900 | Rare:9 | ||||
| chr11:85664577-85664702 | Rare:71 | ||||
| chr11:85664809-85664866 | Rare:17 | ||||
| chr11:85664871-85664934 | Rare:21 | ||||
| chr11:85664970-85665181 | Common:1; Rare:86 | ||||
| chr11:85682842-85682917 | Common:1; Rare:35 | ||||
| chr11:85686087-85686392 | Common:2; Rare:70 | ||||
| chr11:85811100-85811308 | Common:2; Rare:68 |