| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3379114-3379309 | Common:2; Rare:49 | ||||
| chr11:3797494-3797840 | Rare:121 | ||||
| chr11:3808518-3808595 | Common:1; Rare:27 | ||||
| chr11:3840910-3841075 | Rare:73 | ||||
| chr11:3854546-3854611 | Rare:13 | ||||
| chr11:4094730-4094873 | Common:1; Rare:41 | ||||
| chr11:4393658-4393808 | Rare:36 | ||||
| chr11:4608171-4608416 | Common:1; Rare:68 | ||||
| chr11:5624858-5625040 | Rare:35 | ||||
| chr11:6390225-6390421 | Common:2; Rare:56 | ||||
| chr11:6481299-6481558 | Common:5; Rare:120 | ||||
| chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
| chr11:6612239-6612332 | Common:2; Rare:29 | ||||
| chr11:6612655-6612676 | Rare:3 | ||||
| chr11:6683267-6683669 | Common:6; Rare:148 |