| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75549287-75549513 | Common:4; Rare:59 | ||||
| chr13:75549725-75549854 | Common:3; Rare:46 | ||||
| chr13:75636176-75636332 | Common:1; Rare:32 | ||||
| chr13:76885737-76886137 | Common:3; Rare:197 | ||||
| chr13:76886403-76886667 | Common:2; Rare:81 | ||||
| chr13:76992023-76992215 | Common:1; Rare:85; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr13:76992275-76992456 | Common:3; Rare:41; Clinvar (benign):7 | ||||
| chr13:77027114-77027444 | Common:7; Rare:100 | ||||
| chr13:77326028-77326595 | Common:2; Rare:176 | ||||
| chr13:77327066-77327301 | Common:1; Rare:90 | ||||
| chr13:77697391-77697746 | Common:2; Rare:100 | ||||
| chr13:77698350-77698470 | Rare:39 | ||||
| chr13:77698527-77699438 | Common:5; Rare:301 | ||||
| chr13:77918675-77919433 | Common:3; Rare:217 | ||||
| chr13:78659110-78659235 | Common:2; Rare:93 |