| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70398274-70398621 | Common:4; Rare:121 | ||||
| chr11:70661701-70661909 | Rare:71 | ||||
| chr11:70662119-70662425 | Common:1; Rare:75 | ||||
| chr11:71448289-71448702 | Common:4; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452987-71453280 | Common:3; Rare:82 | ||||
| chr11:71787350-71787534 | Common:11; Rare:72 | ||||
| chr11:71928889-71929115 | Common:1; Rare:76 | ||||
| chr11:72040418-72040451 | Common:1; Rare:12 | ||||
| chr11:72040643-72040676 | Common:1; Rare:4 | ||||
| chr11:72040686-72040807 | Rare:23 | ||||
| chr11:72040809-72041295 | Common:1; Rare:103 | ||||
| chr11:72041523-72041573 | Rare:8 | ||||
| chr11:72041846-72041916 | Common:2; Rare:11 | ||||
| chr11:72041934-72042063 | Rare:30 | ||||
| chr11:72042147-72042330 | Rare:30 |