| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65354517-65354804 | Common:1; Rare:84 | ||||
| chr11:65381824-65381976 | Common:1; Rare:52 | ||||
| chr11:65382105-65382304 | Common:2; Rare:44 | ||||
| chr11:65382312-65382640 | Common:3; Rare:71 | ||||
| chr11:65382688-65383005 | Common:1; Rare:47 | ||||
| chr11:65386431-65386715 | Common:1; Rare:88 | ||||
| chr11:65503074-65503160 | Rare:45 | ||||
| chr11:65524844-65525198 | Rare:63 | ||||
| chr11:65525306-65525523 | Rare:42 | ||||
| chr11:65525532-65525605 | Rare:19 | ||||
| chr11:65539856-65540099 | Common:2; Rare:92; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65540222-65540353 | Rare:50 | ||||
| chr11:65540454-65540872 | Common:5; Rare:164 | ||||
| chr11:65540994-65541133 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr11:65558188-65558715 | Common:7; Rare:106 |