| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47176837-47177100 | Common:1; Rare:110 | ||||
| chr11:47214843-47215025 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:47248769-47248955 | Rare:77 | ||||
| chr11:47269117-47269396 | Common:1; Rare:57 | ||||
| chr11:47269545-47269823 | Common:1; Rare:98 | ||||
| chr11:47270018-47270217 | Common:1; Rare:76 | ||||
| chr11:47426406-47426648 | Rare:60 | ||||
| chr11:47553039-47553356 | Common:2; Rare:113 | ||||
| chr11:47565478-47565632 | Common:3; Rare:30 | ||||
| chr11:47578675-47579094 | Common:1; Rare:142; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642447-47642805 | Rare:130 | ||||
| chr11:47848322-47848390 | Rare:34 | ||||
| chr11:57181743-57181975 | Common:1; Rare:74 | ||||
| chr11:57335740-57335953 | Common:4; Rare:49 | ||||
| chr11:57427070-57427259 | Common:1; Rare:57 |