| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32893192-32893423 | Common:1; Rare:55 | ||||
| chr11:33040017-33040020 | Rare:1 | ||||
| chr11:33161443-33161632 | Common:6; Rare:50 | ||||
| chr11:33257184-33257432 | Common:3; Rare:85 | ||||
| chr11:33257621-33257870 | Common:1; Rare:59 | ||||
| chr11:33258464-33258640 | Rare:61 | ||||
| chr11:33736380-33736586 | Common:2; Rare:66 | ||||
| chr11:33774457-33774670 | Common:2; Rare:79 | ||||
| chr11:34052059-34052451 | Common:5; Rare:176 | ||||
| chr11:34438796-34439020 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr11:34620885-34621226 | Common:3; Rare:66 | ||||
| chr11:34624180-34624333 | Common:2; Rare:33 | ||||
| chr11:34642624-34642833 | Common:2; Rare:55 | ||||
| chr11:34916270-34916681 | Common:10; Rare:166; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139381 | Common:1; Rare:118 |