| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214809-47214955 | Common:1; Rare:29 | ||||
| chr11:47214961-47215432 | Common:1; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47215452-47215493 | Rare:12 | ||||
| chr11:47216202-47216446 | Common:1; Rare:82; Clinvar:2 | ||||
| chr11:47248368-47248505 | Common:1; Rare:32 | ||||
| chr11:47248725-47249208 | Common:1; Rare:140 | ||||
| chr11:47269071-47269388 | Common:1; Rare:65 | ||||
| chr11:47269472-47269710 | Common:1; Rare:76 | ||||
| chr11:47269859-47270236 | Common:2; Rare:123 | ||||
| chr11:47377810-47378144 | Common:1; Rare:67 | ||||
| chr11:47378471-47378701 | Rare:44 | ||||
| chr11:47378769-47378893 | Rare:17 | ||||
| chr11:47407933-47408205 | Rare:44 | ||||
| chr11:47408300-47408748 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:47426164-47426268 | Rare:45 |