| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:4393651-4393814 | Rare:41 | ||||
| chr11:5596053-5596120 | Rare:20 | ||||
| chr11:5624889-5625029 | Rare:23 | ||||
| chr11:6234598-6234798 | Common:2; Rare:65 | ||||
| chr11:6390330-6390503 | Common:1; Rare:47 | ||||
| chr11:6473889-6474124 | Rare:71 | ||||
| chr11:6481292-6481524 | Common:4; Rare:92 | ||||
| chr11:6603474-6603835 | Common:4; Rare:111; Clinvar (benign):3 | ||||
| chr11:6619371-6619545 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:7020316-7020500 | Rare:66 | ||||
| chr11:7513611-7513983 | Common:6; Rare:112 | ||||
| chr11:8168980-8169095 | Common:2; Rare:38 | ||||
| chr11:8682644-8682837 | Common:2; Rare:86 | ||||
| chr11:8682955-8683265 | Common:2; Rare:104 | ||||
| chr11:8910928-8911265 | Common:6; Rare:93 |