| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35138954-35139366 | Common:1; Rare:115 | ||||
| chr11:35214851-35215183 | Common:1; Rare:82 | ||||
| chr11:43358813-43359066 | Rare:112 | ||||
| chr11:43680502-43680817 | Common:1; Rare:95 | ||||
| chr11:45917827-45918180 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46119418-46119601 | Common:1; Rare:37 | ||||
| chr11:46120937-46121254 | Common:2; Rare:45 | ||||
| chr11:46345292-46345583 | Common:3; Rare:90 | ||||
| chr11:46700553-46700818 | Common:1; Rare:69 | ||||
| chr11:47214625-47215016 | Common:3; Rare:71; Clinvar:1 | ||||
| chr11:47248783-47248945 | Rare:67 | ||||
| chr11:47257780-47257986 | Rare:40 | ||||
| chr11:47269625-47269674 | Common:1; Rare:14 | ||||
| chr11:47378297-47378699 | Rare:112; Clinvar:1 | ||||
| chr11:47578965-47579112 | Rare:75; Clinvar:2; Clinvar (pathogenic):1 |