| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51222090-51222610 | Common:4; Rare:212 | ||||
| chr13:51451945-51452319 | Common:3; Rare:200 | ||||
| chr13:51452517-51452750 | Common:2; Rare:104 | ||||
| chr13:51452750-51453429 | Common:2; Rare:641 | ||||
| chr13:51453561-51453743 | Common:6; Rare:96 | ||||
| chr13:51583760-51584589 | Common:7; Rare:281 | ||||
| chr13:51584690-51585370 | Common:2; Rare:227 | ||||
| chr13:51803591-51803922 | Rare:189 | ||||
| chr13:51804027-51804293 | Common:6; Rare:177 | ||||
| chr13:52011398-52011565 | Common:2; Rare:52; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:52011969-52012487 | Common:6; Rare:459; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr13:52127760-52128270 | Common:2; Rare:94 | ||||
| chr13:52129039-52129173 | Rare:36 | ||||
| chr13:52158970-52159883 | Common:20; Rare:432 | ||||
| chr13:52449820-52449986 | Rare:32 |