| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28658867-28659227 | Common:2; Rare:136; Clinvar (pathogenic):1 | ||||
| chr13:28659582-28659859 | Common:1; Rare:68 | ||||
| chr13:28718335-28718535 | Rare:28 | ||||
| chr13:28718605-28719230 | Common:4; Rare:157 | ||||
| chr13:29496236-29496458 | Rare:31 | ||||
| chr13:29594289-29595253 | Common:4; Rare:220 | ||||
| chr13:29595328-29595916 | Common:4; Rare:177 | ||||
| chr13:29849400-29850223 | Common:1; Rare:220 | ||||
| chr13:29850228-29850502 | Common:4; Rare:73 | ||||
| chr13:29850509-29850740 | Common:2; Rare:85 | ||||
| chr13:30306773-30306871 | Common:1; Rare:27 | ||||
| chr13:30306989-30307258 | Common:5; Rare:75 | ||||
| chr13:30307368-30307638 | Common:4; Rare:86 | ||||
| chr13:30464186-30465016 | Common:7; Rare:276 | ||||
| chr13:30465088-30465526 | Common:4; Rare:130 |