| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625332-125626061 | Common:5; Rare:221 | ||||
| chr11:125626124-125626468 | Common:1; Rare:93 | ||||
| chr11:125626503-125626627 | Rare:25 | ||||
| chr11:125887513-125887806 | Common:2; Rare:87 | ||||
| chr11:125887857-125888232 | Common:3; Rare:103 | ||||
| chr11:125902967-125903073 | Common:1; Rare:18 | ||||
| chr11:125903112-125903328 | Rare:47 | ||||
| chr11:126062808-126062928 | Common:2; Rare:38 | ||||
| chr11:126062949-126063046 | Common:1; Rare:40 | ||||
| chr11:126063274-126063501 | Common:3; Rare:45; Clinvar (benign):1 | ||||
| chr11:126210658-126211027 | Common:3; Rare:92 | ||||
| chr11:126211199-126211439 | Rare:58 | ||||
| chr11:126211564-126211853 | Rare:135 | ||||
| chr11:126212005-126212095 | Rare:20 | ||||
| chr11:126268448-126268677 | Common:3; Rare:56 |