| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34358340-34358690 | Rare:114 | ||||
| chr11:34438693-34439006 | Common:4; Rare:180; Clinvar (benign):2 | ||||
| chr11:34642137-34642397 | Common:5; Rare:65 | ||||
| chr11:34916000-34916260 | Common:6; Rare:158; Clinvar (benign):4 | ||||
| chr11:34916280-34916681 | Common:20; Rare:320; Clinvar:11; Clinvar (benign):22; Clinvar (pathogenic):2 | ||||
| chr11:35138949-35139245 | Common:2; Rare:127 | ||||
| chr11:35180001-35180450 | Common:6; Rare:167 | ||||
| chr11:35618261-35618459 | Common:1; Rare:62 | ||||
| chr11:35619070-35619520 | Common:2; Rare:275 | ||||
| chr11:35662634-35662974 | Common:5; Rare:183 | ||||
| chr11:35943936-35944119 | Common:6; Rare:121 | ||||
| chr11:36289359-36289529 | Common:3; Rare:123 | ||||
| chr11:36376120-36376560 | Common:5; Rare:152 | ||||
| chr11:36510229-36510353 | Rare:67 | ||||
| chr11:36594314-36594554 | Common:1; Rare:45 |