| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75482122-75482273 | Common:1; Rare:34 | ||||
| chr13:75482593-75482699 | Common:1; Rare:22 | ||||
| chr13:75537564-75538212 | Common:6; Rare:226 | ||||
| chr13:75549346-75549879 | Common:9; Rare:149 | ||||
| chr13:75549930-75549994 | Rare:15 | ||||
| chr13:75636126-75636405 | Common:1; Rare:65 | ||||
| chr13:75636871-75636999 | Common:1; Rare:29 | ||||
| chr13:75760522-75760726 | Common:2; Rare:48 | ||||
| chr13:76886324-76886716 | Common:2; Rare:126 | ||||
| chr13:76991559-76991671 | Rare:22 | ||||
| chr13:76991855-76992260 | Common:4; Rare:167; Clinvar:25; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr13:76992340-76992530 | Common:4; Rare:37 | ||||
| chr13:77026510-77026864 | Common:3; Rare:104 | ||||
| chr13:77027047-77027333 | Common:6; Rare:102 | ||||
| chr13:77027518-77027580 | Rare:16 |