| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62627049-62627348 | Rare:89 | ||||
| chr11:62646560-62646766 | Common:1; Rare:87; Clinvar (pathogenic):1 | ||||
| chr11:62653273-62653436 | Common:1; Rare:51 | ||||
| chr11:62665133-62665333 | Common:4; Rare:92 | ||||
| chr11:62678987-62679308 | Rare:99 | ||||
| chr11:62706102-62706418 | Common:3; Rare:114; Clinvar (benign):6 | ||||
| chr11:62709448-62709645 | Rare:96 | ||||
| chr11:62726970-62727302 | Common:3; Rare:122 | ||||
| chr11:62727435-62727715 | Rare:108 | ||||
| chr11:62728409-62728861 | Common:3; Rare:207 | ||||
| chr11:62753833-62753940 | Common:1; Rare:34 | ||||
| chr11:62754090-62754284 | Common:1; Rare:58 | ||||
| chr11:62761624-62761657 | Rare:15 | ||||
| chr11:62771347-62771463 | Rare:38 | ||||
| chr11:62787292-62787454 | Common:2; Rare:120 |