| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322509-18322616 | Common:2; Rare:50 | ||||
| chr11:18394422-18394615 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr11:18526851-18526972 | Rare:59 | ||||
| chr11:18588672-18588860 | Common:2; Rare:63 | ||||
| chr11:18698494-18698836 | Common:6; Rare:87 | ||||
| chr11:20363651-20363856 | Common:4; Rare:43 | ||||
| chr11:22625813-22625865 | Common:2; Rare:27; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506729-27506857 | Common:1; Rare:60 | ||||
| chr11:28108123-28108421 | Common:1; Rare:91 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509575-31509784 | Common:1; Rare:65 | ||||
| chr11:33161449-33161624 | Common:5; Rare:46 | ||||
| chr11:33257224-33257453 | Common:3; Rare:76 | ||||
| chr11:34620885-34621159 | Common:2; Rare:55 | ||||
| chr11:34916311-34916658 | Common:10; Rare:141; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 |