| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72781300-72781790 | Common:2; Rare:141 | ||||
| chr13:72781832-72782347 | Common:7; Rare:1049 | ||||
| chr13:73058702-73059097 | Common:1; Rare:324 | ||||
| chr13:74134220-74134690 | Common:5; Rare:169 | ||||
| chr13:75326480-75326960 | Common:7; Rare:131 | ||||
| chr13:75481240-75481958 | Common:7; Rare:410; Clinvar:2; Clinvar (benign):4 | ||||
| chr13:75481992-75482692 | Common:16; Rare:316 | ||||
| chr13:75537737-75538195 | Common:18; Rare:529 | ||||
| chr13:75549253-75549840 | Common:56; Rare:787 | ||||
| chr13:75550240-75550610 | Common:1; Rare:74 | ||||
| chr13:75635930-75636430 | Common:5; Rare:263 | ||||
| chr13:76886180-76886860 | Common:11; Rare:274 | ||||
| chr13:76991820-76992280 | Common:21; Rare:765; Clinvar:118; Clinvar (benign):90; Clinvar (pathogenic):19 | ||||
| chr13:76992271-76992451 | Common:3; Rare:39; Clinvar (benign):7 | ||||
| chr13:76992402-76992519 | Common:4; Rare:23 |