| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65386452-65386747 | Common:1; Rare:90 | ||||
| chr11:65570415-65570494 | Rare:35 | ||||
| chr11:65614175-65614393 | Rare:49 | ||||
| chr11:65662890-65663086 | Common:1; Rare:50 | ||||
| chr11:65857036-65857309 | Common:3; Rare:83 | ||||
| chr11:65888426-65888565 | Rare:57 | ||||
| chr11:65890492-65890670 | Common:2; Rare:59 | ||||
| chr11:65900389-65900681 | Common:2; Rare:64 | ||||
| chr11:66002087-66002528 | Common:3; Rare:125; Clinvar:8; Clinvar (benign):3 | ||||
| chr11:66011707-66012109 | Common:2; Rare:99 | ||||
| chr11:66058084-66058383 | Rare:74 | ||||
| chr11:66347630-66347823 | Common:5; Rare:49 | ||||
| chr11:66480239-66480446 | Common:1; Rare:55 | ||||
| chr11:66510617-66510671 | Rare:35; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:66593050-66593220 | Common:1; Rare:62 |