| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22192929-22193104 | Rare:40 | ||||
| chr11:22625800-22625984 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829262-22829437 | Common:1; Rare:48 | ||||
| chr11:22829760-22830108 | Common:4; Rare:114 | ||||
| chr11:27363194-27363338 | Rare:56 | ||||
| chr11:27472742-27472945 | Common:1; Rare:45 | ||||
| chr11:27506577-27506954 | Common:1; Rare:146 | ||||
| chr11:27700448-27700611 | Common:2; Rare:39 | ||||
| chr11:27701540-27701685 | Rare:28 | ||||
| chr11:27701830-27702030 | Rare:45 | ||||
| chr11:27719250-27719650 | Common:1; Rare:122 | ||||
| chr11:28107595-28107852 | Common:1; Rare:40 | ||||
| chr11:28108053-28108462 | Common:3; Rare:120 | ||||
| chr11:28110175-28110371 | Rare:49 | ||||
| chr11:30322912-30323174 | Common:2; Rare:77 |