| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94493486-94493597 | Rare:28 | ||||
| chr11:94493779-94494080 | Common:6; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94543811-94543951 | Common:3; Rare:34 | ||||
| chr11:94567285-94567398 | Common:1; Rare:27 | ||||
| chr11:94768277-94768423 | Rare:42 | ||||
| chr11:94973497-94973767 | Rare:81 | ||||
| chr11:95066778-95066956 | Rare:32 | ||||
| chr11:95067432-95067626 | Common:1; Rare:82 | ||||
| chr11:95089719-95089949 | Common:3; Rare:96 | ||||
| chr11:95231038-95231587 | Common:3; Rare:176 | ||||
| chr11:95232414-95232615 | Common:2; Rare:32 | ||||
| chr11:95789414-95789950 | Common:4; Rare:234 | ||||
| chr11:95790175-95790727 | Common:4; Rare:201; Clinvar:2 | ||||
| chr11:95791031-95791081 | Rare:10 | ||||
| chr11:95923771-95924172 | Common:2; Rare:163; Clinvar:5; Clinvar (benign):5 |