| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65662902-65663017 | Common:1; Rare:30 | ||||
| chr11:65857211-65857334 | Rare:33 | ||||
| chr11:65860178-65860549 | Common:3; Rare:124 | ||||
| chr11:65888378-65888678 | Common:1; Rare:102 | ||||
| chr11:65900308-65900551 | Common:4; Rare:49 | ||||
| chr11:65919032-65919280 | Rare:91 | ||||
| chr11:65921064-65921381 | Common:1; Rare:79 | ||||
| chr11:66002134-66002521 | Common:3; Rare:103; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66345038-66345442 | Common:1; Rare:106 | ||||
| chr11:66347586-66347800 | Common:3; Rare:53 | ||||
| chr11:66480222-66480446 | Common:2; Rare:60 | ||||
| chr11:66566144-66566346 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:66593044-66593244 | Common:1; Rare:74 | ||||
| chr11:66843334-66843464 | Common:5; Rare:64 | ||||
| chr11:67443441-67443572 | Common:1; Rare:41 |