| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62665165-62665309 | Common:3; Rare:56 | ||||
| chr11:62855881-62856004 | Rare:54 | ||||
| chr11:64226141-64226318 | Common:2; Rare:49 | ||||
| chr11:64245575-64245924 | Common:2; Rare:73 | ||||
| chr11:64284643-64284819 | Rare:82 | ||||
| chr11:64317469-64317629 | Common:3; Rare:61 | ||||
| chr11:64317985-64318291 | Rare:126 | ||||
| chr11:65014049-65014228 | Rare:43 | ||||
| chr11:65570373-65570494 | Rare:52 | ||||
| chr11:66002134-66002532 | Common:3; Rare:107; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66480228-66480438 | Common:1; Rare:55 | ||||
| chr11:67482901-67483148 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68903800-68903923 | Common:3; Rare:53; Clinvar (benign):3 | ||||
| chr11:70398431-70398601 | Common:2; Rare:62 | ||||
| chr11:71448379-71448690 | Common:3; Rare:78; Clinvar (benign):1 |