| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322521-18322645 | Common:1; Rare:54 | ||||
| chr11:18394405-18394619 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr11:18396204-18396419 | Rare:76 | ||||
| chr11:18526841-18527025 | Common:1; Rare:94 | ||||
| chr11:18588672-18588860 | Common:2; Rare:63 | ||||
| chr11:18634332-18634580 | Common:2; Rare:79 | ||||
| chr11:18698689-18698772 | Common:1; Rare:27 | ||||
| chr11:18791539-18791905 | Common:1; Rare:119 | ||||
| chr11:20387392-20387771 | Common:8; Rare:123 | ||||
| chr11:20669411-20669670 | Common:3; Rare:98 | ||||
| chr11:22338190-22338545 | Common:1; Rare:87 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496504-24496691 | Common:1; Rare:28 | ||||
| chr11:24496915-24497305 | Common:3; Rare:111 | ||||
| chr11:26331957-26332182 | Common:3; Rare:69 |