| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124889433-124889706 | Common:4; Rare:35 | ||||
| chr11:124891115-124891474 | Common:3; Rare:96; Clinvar (pathogenic):1 | ||||
| chr11:124900609-124900820 | Common:1; Rare:43 | ||||
| chr11:125058932-125059008 | Common:1; Rare:13 | ||||
| chr11:125328350-125328391 | Common:2; Rare:11 | ||||
| chr11:126067614-126067809 | Rare:33 | ||||
| chr11:126067963-126068015 | Rare:10 | ||||
| chr11:126205446-126205481 | Common:1; Rare:16 | ||||
| chr11:126226726-126226741 | Rare:1 | ||||
| chr11:126261258-126261483 | Common:2; Rare:50 | ||||
| chr11:126268061-126268211 | Rare:41 | ||||
| chr11:126270099-126270399 | Common:1; Rare:47 | ||||
| chr11:126304259-126304338 | Common:1; Rare:37 | ||||
| chr11:126354706-126354774 | Rare:12 | ||||
| chr11:128334248-128334358 | Common:1; Rare:18 |