| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32428323-32428547 | Rare:57; Clinvar:5; Clinvar (benign):2 | ||||
| chr11:32435529-32435604 | Common:1; Rare:11 | ||||
| chr11:32435620-32435832 | Rare:70 | ||||
| chr11:32435853-32436000 | Common:1; Rare:29 | ||||
| chr11:33039443-33039757 | Common:1; Rare:75 | ||||
| chr11:33161388-33161648 | Common:7; Rare:65 | ||||
| chr11:33257147-33257427 | Common:3; Rare:94 | ||||
| chr11:33736391-33736572 | Common:2; Rare:62 | ||||
| chr11:34051622-34051741 | Rare:53 | ||||
| chr11:34105481-34105697 | Common:2; Rare:74 | ||||
| chr11:34358005-34358312 | Common:2; Rare:83 | ||||
| chr11:34438776-34439023 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr11:34620933-34621115 | Common:1; Rare:33 | ||||
| chr11:34916292-34916669 | Common:10; Rare:154; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35525581-35525804 | Rare:55 |