| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:695712-695825 | Rare:40 | ||||
| chr11:705126-705223 | Common:1; Rare:26 | ||||
| chr11:705985-706262 | Common:2; Rare:91 | ||||
| chr11:706517-706629 | Rare:17 | ||||
| chr11:721096-721411 | Rare:135 | ||||
| chr11:726145-726444 | Common:2; Rare:128 | ||||
| chr11:747284-747565 | Rare:121; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:763995-764430 | Common:4; Rare:116; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:764706-764842 | Common:1; Rare:47; Clinvar:1 | ||||
| chr11:777451-777619 | Common:1; Rare:75 | ||||
| chr11:809469-809647 | Common:2; Rare:49 | ||||
| chr11:809799-810038 | Common:2; Rare:110 | ||||
| chr11:827239-827389 | Common:3; Rare:42 | ||||
| chr11:827539-827622 | Common:2; Rare:22 | ||||
| chr11:832858-833018 | Common:7; Rare:58 |