| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1840006-1840152 | Rare:28 | ||||
| chr11:1876417-1876466 | Rare:13 | ||||
| chr11:2138323-2138585 | Common:2; Rare:63 | ||||
| chr11:2885702-2885806 | Rare:40; Clinvar:1 | ||||
| chr11:3057363-3057552 | Rare:68 | ||||
| chr11:3855535-3855754 | Common:2; Rare:45 | ||||
| chr11:4393658-4393820 | Rare:38 | ||||
| chr11:5624889-5625024 | Rare:20 | ||||
| chr11:6234618-6234793 | Common:2; Rare:54 | ||||
| chr11:6319745-6319775 | Rare:9 | ||||
| chr11:6319782-6319942 | Rare:36 | ||||
| chr11:6320490-6320623 | Common:2; Rare:45 | ||||
| chr11:6390225-6390494 | Common:2; Rare:77 | ||||
| chr11:6481299-6481536 | Common:4; Rare:102 | ||||
| chr11:6603536-6603860 | Common:4; Rare:97; Clinvar (benign):3 |