| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:506337-506466 | Common:2; Rare:32 | ||||
| chr11:506607-506710 | Rare:23 | ||||
| chr11:506732-507001 | Common:3; Rare:92 | ||||
| chr11:507164-507581 | Common:4; Rare:135 | ||||
| chr11:535418-535786 | Common:7; Rare:153; Clinvar (benign):1 | ||||
| chr11:560703-561021 | Common:6; Rare:146 | ||||
| chr11:576420-576531 | Rare:44 | ||||
| chr11:615935-616108 | Common:1; Rare:54 | ||||
| chr11:695756-695821 | Rare:25 | ||||
| chr11:706517-706629 | Rare:17 | ||||
| chr11:747260-747566 | Rare:131; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:764064-764418 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:777460-777635 | Common:1; Rare:79 | ||||
| chr11:796190-796534 | Common:1; Rare:95; Clinvar:1 | ||||
| chr11:809498-809786 | Common:3; Rare:86 |