| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846152-46846421 | Common:1; Rare:85 | ||||
| chr11:47185366-47185534 | Common:2; Rare:39 | ||||
| chr11:47214331-47214515 | Common:1; Rare:17 | ||||
| chr11:47214843-47215165 | Common:2; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248766-47248970 | Rare:82 | ||||
| chr11:47257663-47258011 | Rare:57 | ||||
| chr11:47408366-47408655 | Common:1; Rare:86; Clinvar (benign):2 | ||||
| chr11:47471988-47472234 | Rare:51 | ||||
| chr11:47553003-47553281 | Common:3; Rare:104 | ||||
| chr11:47565025-47565298 | Rare:44 | ||||
| chr11:47565382-47565413 | Rare:4 | ||||
| chr11:47565420-47565717 | Common:4; Rare:63 | ||||
| chr11:47578932-47579335 | Rare:191; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47594358-47594538 | Common:1; Rare:55 | ||||
| chr11:47638711-47639051 | Common:5; Rare:90 |