| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124800402-124800471 | Rare:24 | ||||
| chr11:124953948-124954215 | Common:5; Rare:77 | ||||
| chr11:125063168-125063394 | Common:3; Rare:73 | ||||
| chr11:125111710-125112006 | Common:3; Rare:60 | ||||
| chr11:125164499-125164754 | Rare:49 | ||||
| chr11:125569196-125569545 | Common:2; Rare:101 | ||||
| chr11:125592456-125592930 | Common:6; Rare:160 | ||||
| chr11:125625867-125626007 | Rare:44 | ||||
| chr11:125626248-125626549 | Common:3; Rare:76 | ||||
| chr11:125887468-125887745 | Common:2; Rare:88 | ||||
| chr11:125903172-125903328 | Rare:37 | ||||
| chr11:125904269-125904515 | Rare:78 | ||||
| chr11:126211641-126211822 | Rare:84 | ||||
| chr11:126268761-126269207 | Common:2; Rare:174; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126283039-126283131 | Rare:40 |