| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124762259-124762431 | Rare:42 | ||||
| chr11:124800406-124800485 | Rare:31 | ||||
| chr11:124876727-124876897 | Common:3; Rare:38 | ||||
| chr11:124897801-124898171 | Common:5; Rare:74 | ||||
| chr11:124953948-124954364 | Common:5; Rare:106 | ||||
| chr11:125111552-125112047 | Common:4; Rare:120 | ||||
| chr11:125164494-125164759 | Rare:50 | ||||
| chr11:125452781-125452886 | Rare:19 | ||||
| chr11:125496191-125496537 | Rare:74 | ||||
| chr11:125569420-125569545 | Common:1; Rare:42 | ||||
| chr11:125592538-125592939 | Common:6; Rare:130; Clinvar (benign):1 | ||||
| chr11:125625864-125626007 | Rare:45 | ||||
| chr11:125680825-125681208 | Common:2; Rare:57 | ||||
| chr11:125883528-125883654 | Rare:32; Clinvar:2 | ||||
| chr11:125887212-125887263 | Rare:14 |