| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70416056-70416323 | Common:2; Rare:53 | ||||
| chr11:71240920-71241156 | Rare:38 | ||||
| chr11:71241262-71241362 | Rare:17 | ||||
| chr11:71448323-71448671 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452395-71452475 | Common:1; Rare:8 | ||||
| chr11:71452954-71453172 | Common:4; Rare:56 | ||||
| chr11:71786759-71787092 | Common:2; Rare:98 | ||||
| chr11:71787216-71787739 | Common:21; Rare:215 | ||||
| chr11:71927944-71928009 | Common:1; Rare:11 | ||||
| chr11:71928155-71928297 | Common:1; Rare:28 | ||||
| chr11:71928361-71928509 | Rare:40 | ||||
| chr11:71928559-71928722 | Rare:44 | ||||
| chr11:71928724-71929110 | Common:1; Rare:110 | ||||
| chr11:72040673-72040932 | Common:1; Rare:56 | ||||
| chr11:72041094-72041343 | Common:1; Rare:46 |