| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33868624-33869284 | Common:5; Rare:197 | ||||
| chr11:33869589-33871545 | Common:32; Rare:1129 | ||||
| chr11:33891743-33892188 | Common:3; Rare:161 | ||||
| chr11:34051175-34051782 | Common:1; Rare:812 | ||||
| chr11:34051956-34052772 | Common:32; Rare:1321 | ||||
| chr11:34052993-34053573 | Common:7; Rare:405 | ||||
| chr11:34104659-34105386 | Common:1; Rare:258 | ||||
| chr11:34105344-34105768 | Common:22; Rare:708 | ||||
| chr11:34105900-34106040 | Common:2; Rare:36 | ||||
| chr11:34106136-34106536 | Common:4; Rare:95 | ||||
| chr11:34242041-34242441 | Common:2; Rare:90 | ||||
| chr11:34358005-34358164 | Common:1; Rare:53 | ||||
| chr11:34358283-34358683 | Rare:76 | ||||
| chr11:34438466-34439200 | Common:19; Rare:846; Clinvar (benign):5 | ||||
| chr11:34439164-34439644 | Common:3; Rare:176 |