| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31509575-31509787 | Common:1; Rare:65 | ||||
| chr11:33015784-33015915 | Rare:49 | ||||
| chr11:33039681-33040015 | Common:2; Rare:87 | ||||
| chr11:33161381-33161686 | Common:7; Rare:78 | ||||
| chr11:33257195-33257427 | Common:3; Rare:78 | ||||
| chr11:33722637-33722844 | Common:2; Rare:41 | ||||
| chr11:33736384-33736607 | Common:2; Rare:69 | ||||
| chr11:34051617-34051741 | Rare:54 | ||||
| chr11:34052159-34052493 | Common:4; Rare:156 | ||||
| chr11:34105481-34105719 | Common:2; Rare:78 | ||||
| chr11:34438784-34439009 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr11:34916263-34916678 | Common:11; Rare:165; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:34977500-34977826 | Common:1; Rare:60 | ||||
| chr11:35138954-35139366 | Common:1; Rare:115 | ||||
| chr11:35943936-35944116 | Common:3; Rare:61 |