| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526821-18527001 | Common:1; Rare:82 | ||||
| chr11:18588612-18588905 | Common:2; Rare:104 | ||||
| chr11:18634260-18634570 | Common:3; Rare:110 | ||||
| chr11:18634763-18634869 | Rare:25 | ||||
| chr11:19240828-19241298 | Rare:135 | ||||
| chr11:20363452-20363811 | Common:5; Rare:64 | ||||
| chr11:20363837-20364430 | Common:7; Rare:168 | ||||
| chr11:20387472-20387774 | Common:5; Rare:98 | ||||
| chr11:22192901-22193100 | Rare:42 | ||||
| chr11:22625803-22626002 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:27362838-27363137 | Common:2; Rare:127 | ||||
| chr11:27363169-27363286 | Rare:53 | ||||
| chr11:27472121-27472485 | Common:1; Rare:91 | ||||
| chr11:27472661-27473036 | Common:3; Rare:90 | ||||
| chr11:27506718-27506859 | Common:1; Rare:67 |