| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75636004-75636374 | Common:2; Rare:91 | ||||
| chr13:75804030-75804541 | Common:4; Rare:125 | ||||
| chr13:76991951-76992220 | Common:4; Rare:128; Clinvar:22; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr13:77027141-77027287 | Common:5; Rare:43 | ||||
| chr13:77327060-77327161 | Rare:46 | ||||
| chr13:77918567-77918949 | Common:2; Rare:85; Clinvar (benign):2 | ||||
| chr13:77919397-77919599 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:78659097-78659234 | Common:2; Rare:99 | ||||
| chr13:79405704-79405898 | Common:1; Rare:61 | ||||
| chr13:79406219-79406339 | Common:3; Rare:38 | ||||
| chr13:79481003-79481467 | Common:2; Rare:180 | ||||
| chr13:80339907-80339991 | Common:1; Rare:26 | ||||
| chr13:80341303-80341484 | Rare:56 | ||||
| chr13:93226960-93227439 | Common:1; Rare:112; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:94596106-94596300 | Common:1; Rare:76 |