| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65570293-65570494 | Rare:75 | ||||
| chr11:65575850-65576060 | Common:3; Rare:60 | ||||
| chr11:65581273-65581786 | Common:3; Rare:147 | ||||
| chr11:65591770-65591812 | Common:4; Rare:12 | ||||
| chr11:65614216-65614329 | Rare:23 | ||||
| chr11:65615664-65615842 | Common:2; Rare:67 | ||||
| chr11:65650241-65650449 | Rare:65 | ||||
| chr11:65662890-65663095 | Common:1; Rare:52 | ||||
| chr11:65663398-65663475 | Common:1; Rare:17 | ||||
| chr11:65711869-65712270 | Common:1; Rare:136 | ||||
| chr11:65856996-65857319 | Common:4; Rare:98 | ||||
| chr11:65860172-65860754 | Common:3; Rare:187 | ||||
| chr11:65872682-65872961 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:65873549-65873791 | Common:3; Rare:78 | ||||
| chr11:65888402-65888676 | Common:1; Rare:95 |