| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111541279-111541339 | Rare:21 | ||||
| chr11:111766357-111766426 | Rare:35 | ||||
| chr11:111814679-111814886 | Common:1; Rare:31 | ||||
| chr11:111871253-111871376 | Rare:40; Clinvar:1 | ||||
| chr11:111879158-111879548 | Common:1; Rare:117 | ||||
| chr11:111912712-111912788 | Rare:9 | ||||
| chr11:111912895-111912916 | Rare:5 | ||||
| chr11:111913117-111913294 | Rare:46 | ||||
| chr11:111937134-111937217 | Common:2; Rare:22 | ||||
| chr11:111976689-111976927 | Rare:38 | ||||
| chr11:111977129-111977427 | Common:5; Rare:72 | ||||
| chr11:111977728-111977793 | Rare:16 | ||||
| chr11:112025339-112025611 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:112073995-112074349 | Common:1; Rare:72 | ||||
| chr11:112086720-112086938 | Rare:94; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 |