| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65382494-65382872 | Common:1; Rare:63 | ||||
| chr11:65386400-65386724 | Common:1; Rare:92 | ||||
| chr11:65524791-65525177 | Rare:76 | ||||
| chr11:65540614-65540852 | Common:3; Rare:102 | ||||
| chr11:65546532-65546909 | Common:3; Rare:123; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65569866-65570151 | Common:1; Rare:93 | ||||
| chr11:65570177-65570528 | Common:2; Rare:126 | ||||
| chr11:65575560-65575781 | Rare:27 | ||||
| chr11:65575826-65576136 | Common:3; Rare:88 | ||||
| chr11:65614145-65614537 | Rare:89 | ||||
| chr11:65615041-65615071 | Rare:4 | ||||
| chr11:65615604-65615893 | Common:2; Rare:101 | ||||
| chr11:65616023-65616092 | Rare:16 | ||||
| chr11:65637912-65638251 | Common:4; Rare:114 | ||||
| chr11:65638549-65638988 | Common:2; Rare:95 |