| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111299659-111299772 | Common:2; Rare:28 | ||||
| chr11:111766338-111766459 | Common:1; Rare:76 | ||||
| chr11:111871275-111871342 | Rare:20 | ||||
| chr11:111871478-111871629 | Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878645-111879006 | Common:2; Rare:111 | ||||
| chr11:111879154-111879548 | Common:1; Rare:119 | ||||
| chr11:111911928-111912004 | Common:1; Rare:15 | ||||
| chr11:111912006-111912050 | Rare:11 | ||||
| chr11:111912708-111912765 | Rare:6 | ||||
| chr11:111913148-111913269 | Rare:37 | ||||
| chr11:111926988-111927273 | Common:9; Rare:53 | ||||
| chr11:111937078-111937461 | Common:7; Rare:110 | ||||
| chr11:112025315-112025616 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:112073987-112074349 | Common:1; Rare:76 | ||||
| chr11:112086729-112086905 | Rare:71; Clinvar:1 |