| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47426425-47426693 | Rare:60 | ||||
| chr11:47426857-47426978 | Common:1; Rare:24 | ||||
| chr11:47552370-47552806 | Common:5; Rare:153 | ||||
| chr11:47552811-47552944 | Common:1; Rare:47 | ||||
| chr11:47553048-47553407 | Common:2; Rare:118 | ||||
| chr11:47565316-47565708 | Common:4; Rare:76 | ||||
| chr11:47565784-47565904 | Common:1; Rare:50 | ||||
| chr11:47566123-47566246 | Rare:24 | ||||
| chr11:47578173-47578431 | Rare:48 | ||||
| chr11:47578552-47578770 | Rare:58 | ||||
| chr11:47578888-47579144 | Rare:129; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642020-47642127 | Rare:33 | ||||
| chr11:47642151-47642273 | Rare:24 | ||||
| chr11:47642356-47642839 | Rare:155 | ||||
| chr11:47715226-47715469 | Common:1; Rare:58 |