| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64566590-64566860 | Common:1; Rare:89 | ||||
| chr11:64729779-64730179 | Common:2; Rare:226; Clinvar (benign):1 | ||||
| chr11:64842760-64843050 | Rare:105 | ||||
| chr11:65014802-65015062 | Common:2; Rare:45 | ||||
| chr11:65016420-65017610 | Common:14; Rare:369 | ||||
| chr11:65150730-65151060 | Common:5; Rare:133 | ||||
| chr11:65174450-65174960 | Common:3; Rare:129 | ||||
| chr11:65219762-65219919 | Rare:26 | ||||
| chr11:65388380-65389164 | Common:9; Rare:236 | ||||
| chr11:65416441-65416603 | Common:1; Rare:54 | ||||
| chr11:65417025-65417425 | Common:2; Rare:133 | ||||
| chr11:65417909-65418248 | Common:2; Rare:89 | ||||
| chr11:65418210-65418610 | Common:29; Rare:166 | ||||
| chr11:65418651-65419340 | Common:6; Rare:348 | ||||
| chr11:65419973-65420392 | Rare:181 |