| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50909632-50909929 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr13:50909961-50910422 | Common:2; Rare:124; Clinvar:2 | ||||
| chr13:51222217-51222421 | Common:2; Rare:75 | ||||
| chr13:51451529-51452111 | Common:2; Rare:194 | ||||
| chr13:51452979-51453458 | Common:1; Rare:187 | ||||
| chr13:51453468-51453783 | Common:3; Rare:90 | ||||
| chr13:51454099-51454376 | Rare:65 | ||||
| chr13:51583709-51584627 | Common:6; Rare:261 | ||||
| chr13:51584701-51584972 | Common:1; Rare:82 | ||||
| chr13:51803468-51803619 | Common:1; Rare:27 | ||||
| chr13:51803665-51804403 | Common:2; Rare:209 | ||||
| chr13:51979073-51979270 | Common:1; Rare:34 | ||||
| chr13:52011344-52011474 | Common:2; Rare:55; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:52011908-52011993 | Rare:30 | ||||
| chr13:52011997-52012501 | Common:2; Rare:186; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |