| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108223268-108223465 | Rare:53 | ||||
| chr11:108929406-108929653 | Common:1; Rare:45 | ||||
| chr11:111514721-111514887 | Common:2; Rare:66 | ||||
| chr11:111540463-111540685 | Common:1; Rare:50 | ||||
| chr11:111540686-111540928 | Common:2; Rare:86 | ||||
| chr11:111541283-111541560 | Common:2; Rare:65 | ||||
| chr11:111541702-111541931 | Rare:45 | ||||
| chr11:111766307-111766459 | Common:1; Rare:100 | ||||
| chr11:111871264-111871348 | Rare:24 | ||||
| chr11:111879147-111879537 | Rare:120 | ||||
| chr11:112025300-112025560 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:112073994-112074365 | Common:1; Rare:78 | ||||
| chr11:112086700-112086928 | Rare:102; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:112228273-112228672 | Rare:95; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:112961372-112961615 | Common:4; Rare:107 |