| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846148-46846467 | Common:1; Rare:103 | ||||
| chr11:46936591-46936994 | Common:2; Rare:107 | ||||
| chr11:47176266-47176423 | Rare:40 | ||||
| chr11:47176788-47177186 | Common:1; Rare:169 | ||||
| chr11:47177410-47177688 | Rare:45 | ||||
| chr11:47186405-47186544 | Rare:38 | ||||
| chr11:47186930-47187048 | Rare:26 | ||||
| chr11:47214314-47214505 | Common:1; Rare:21 | ||||
| chr11:47214827-47215441 | Common:2; Rare:167; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47216202-47216447 | Common:1; Rare:82; Clinvar:2 | ||||
| chr11:47248303-47248515 | Common:1; Rare:44 | ||||
| chr11:47248697-47248979 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr11:47249102-47249231 | Common:1; Rare:25 | ||||
| chr11:47268932-47269403 | Common:1; Rare:89 | ||||
| chr11:47269458-47269706 | Common:1; Rare:76 |