| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132335194-132335828 | Common:12; Rare:143 | ||||
| chr10:132337014-132337392 | Common:4; Rare:91 | ||||
| chr10:132537489-132537889 | Common:2; Rare:126 | ||||
| chr10:133275692-133275847 | Rare:29 | ||||
| chr10:133275871-133276185 | Common:1; Rare:69 | ||||
| chr10:133276500-133276553 | Rare:14 | ||||
| chr10:133276703-133277012 | Common:1; Rare:80 | ||||
| chr10:133308807-133308994 | Rare:84 | ||||
| chr10:133309077-133309406 | Common:2; Rare:121 | ||||
| chr10:133357667-133357847 | Common:1; Rare:30 | ||||
| chr10:133373258-133373568 | Common:2; Rare:132; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133378948-133379354 | Common:20; Rare:78 | ||||
| chr10:133379445-133379698 | Rare:62 | ||||
| chr10:133390031-133390537 | Common:4; Rare:94 | ||||
| chr10:133393958-133394607 | Common:3; Rare:247 |