| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18634300-18634575 | Common:3; Rare:91 | ||||
| chr11:18634785-18634861 | Rare:15 | ||||
| chr11:18698448-18698764 | Common:4; Rare:76 | ||||
| chr11:20387394-20387765 | Common:8; Rare:120 | ||||
| chr11:22625522-22625609 | Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22626002 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829357-22829422 | Common:1; Rare:18 | ||||
| chr11:26994030-26994200 | Common:1; Rare:30 | ||||
| chr11:26994344-26994617 | Common:1; Rare:66 | ||||
| chr11:27506721-27506852 | Common:1; Rare:63 | ||||
| chr11:28108154-28108414 | Common:1; Rare:74 | ||||
| chr11:30322981-30323164 | Common:1; Rare:52 | ||||
| chr11:30583992-30584136 | Rare:39 | ||||
| chr11:30584159-30584165 | |||||
| chr11:31369744-31369905 | Rare:49 |