| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51584664-51585340 | Common:2; Rare:274 | ||||
| chr13:51803570-51803900 | Rare:330 | ||||
| chr13:51803986-51804386 | Common:10; Rare:331 | ||||
| chr13:51804621-51805021 | Common:1; Rare:76 | ||||
| chr13:51861706-51862131 | Rare:164 | ||||
| chr13:51974397-51974797 | Rare:123; Clinvar:11; Clinvar (pathogenic):4 | ||||
| chr13:51978910-51979330 | Common:8; Rare:228 | ||||
| chr13:52010790-52011730 | Common:8; Rare:414; Clinvar:18; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr13:52012033-52012499 | Common:14; Rare:952; Clinvar:10; Clinvar (benign):2 | ||||
| chr13:52127609-52128009 | Common:1; Rare:143 | ||||
| chr13:52128297-52128697 | Common:4; Rare:138 | ||||
| chr13:52128830-52129323 | Common:3; Rare:270 | ||||
| chr13:52158997-52159397 | Common:7; Rare:75 | ||||
| chr13:52159390-52159893 | Common:8; Rare:309 | ||||
| chr13:52449720-52450370 | Common:6; Rare:317 |