| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52653085-52653164 | Rare:29 | ||||
| chr13:60397110-60397396 | Common:4; Rare:107 | ||||
| chr13:67230293-67230446 | Rare:42 | ||||
| chr13:71867246-71867481 | Common:1; Rare:56 | ||||
| chr13:72727548-72727955 | Common:7; Rare:160 | ||||
| chr13:72781698-72782261 | Common:1; Rare:203 | ||||
| chr13:73058703-73059030 | Rare:107 | ||||
| chr13:75482113-75482551 | Common:6; Rare:103 | ||||
| chr13:75482567-75482608 | Rare:5 | ||||
| chr13:75537662-75537690 | Rare:5 | ||||
| chr13:75549352-75549987 | Common:9; Rare:178 | ||||
| chr13:75635782-75635820 | Rare:6 | ||||
| chr13:75636033-75636365 | Common:2; Rare:76 | ||||
| chr13:76886406-76886673 | Common:2; Rare:82 | ||||
| chr13:76991956-76992194 | Common:3; Rare:114; Clinvar:20; Clinvar (benign):12; Clinvar (pathogenic):3 |