| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68271871-68272134 | Common:2; Rare:108 | ||||
| chr11:68903770-68903937 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69293975-69294170 | Common:3; Rare:24 | ||||
| chr11:69299141-69299216 | Common:1; Rare:15 | ||||
| chr11:69640972-69641240 | Common:1; Rare:55 | ||||
| chr11:69675289-69675503 | Rare:61 | ||||
| chr11:70203116-70203343 | Common:4; Rare:86 | ||||
| chr11:70398448-70398591 | Common:1; Rare:47 | ||||
| chr11:71448337-71448690 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:72080471-72080634 | Rare:33; Clinvar:2 | ||||
| chr11:72103220-72103531 | Rare:90 | ||||
| chr11:72112264-72112539 | Rare:69 | ||||
| chr11:72112655-72112823 | Common:1; Rare:74 | ||||
| chr11:73597986-73598281 | Common:3; Rare:75 | ||||
| chr11:73876799-73877019 | Common:4; Rare:55 |