| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131710795-131711131 | Common:1; Rare:93 | ||||
| chr12:131928963-131929296 | Common:10; Rare:104; Clinvar:1 | ||||
| chr12:132687303-132687789 | Common:5; Rare:176; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887553-132887794 | Rare:74 | ||||
| chr12:132956252-132956421 | Common:1; Rare:37 | ||||
| chr12:132986273-132986448 | Rare:44 | ||||
| chr12:133080733-133080950 | Rare:67 | ||||
| chr12:133130255-133130662 | Common:7; Rare:138 | ||||
| chr13:19782927-19783090 | Common:2; Rare:57 | ||||
| chr13:19863448-19863786 | Common:5; Rare:110 | ||||
| chr13:19958990-19959038 | Common:1; Rare:20 | ||||
| chr13:20525756-20525941 | Common:1; Rare:72 | ||||
| chr13:20566807-20567236 | Common:1; Rare:125 | ||||
| chr13:21140411-21140657 | Rare:110 | ||||
| chr13:21176531-21176717 | Common:1; Rare:91 |