| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207905-17208098 | Common:2; Rare:76 | ||||
| chr11:17389294-17389481 | Common:2; Rare:37 | ||||
| chr11:17719291-17719571 | Common:5; Rare:62 | ||||
| chr11:18266001-18266295 | Common:3; Rare:68 | ||||
| chr11:18322131-18322312 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322508-18322616 | Common:2; Rare:50 | ||||
| chr11:18396113-18396380 | Common:1; Rare:101 | ||||
| chr11:18526812-18526983 | Rare:80 | ||||
| chr11:18588672-18588905 | Common:2; Rare:78 | ||||
| chr11:20363657-20363759 | Common:1; Rare:22 | ||||
| chr11:20363853-20364200 | Common:7; Rare:72 | ||||
| chr11:22625817-22626002 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994094-26994168 | Common:1; Rare:11 | ||||
| chr11:27506738-27506859 | Common:1; Rare:52 | ||||
| chr11:28108134-28108416 | Common:1; Rare:83 |