| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65382636-65382774 | Rare:20 | ||||
| chr11:65386408-65386710 | Common:1; Rare:89 | ||||
| chr11:65524783-65525192 | Rare:81 | ||||
| chr11:65525315-65525560 | Rare:52 | ||||
| chr11:65539825-65540039 | Common:2; Rare:87; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65540607-65540817 | Common:3; Rare:85 | ||||
| chr11:65546532-65546883 | Common:3; Rare:115; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65557315-65557663 | Common:1; Rare:70 | ||||
| chr11:65557759-65558039 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
| chr11:65558180-65558392 | Rare:45 | ||||
| chr11:65558509-65558726 | Common:4; Rare:43 | ||||
| chr11:65569892-65570153 | Common:1; Rare:88 | ||||
| chr11:65570239-65570529 | Common:2; Rare:107 | ||||
| chr11:65572446-65572593 | Rare:48 | ||||
| chr11:65575865-65576100 | Common:3; Rare:71 |