| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124093532-124093733 | Common:2; Rare:39 | ||||
| chr10:125719456-125719761 | Common:1; Rare:108 | ||||
| chr10:125823240-125823573 | Rare:107 | ||||
| chr10:125896474-125896589 | Rare:4 | ||||
| chr10:126905297-126905465 | Rare:64 | ||||
| chr10:128047442-128047628 | Common:2; Rare:60 | ||||
| chr10:132331816-132332214 | Common:13; Rare:128 | ||||
| chr10:133308821-133308989 | Rare:81 | ||||
| chr11:207363-207526 | Common:4; Rare:66 | ||||
| chr11:208633-208847 | Rare:78 | ||||
| chr11:236331-236474 | Common:6; Rare:41 | ||||
| chr11:236834-237051 | Common:2; Rare:80 | ||||
| chr11:320564-320929 | Common:5; Rare:140; Clinvar:1 | ||||
| chr11:506732-507001 | Common:3; Rare:92 |