| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51584719-51584819 | Rare:30 | ||||
| chr13:51803677-51803836 | Rare:45 | ||||
| chr13:51804074-51804227 | Common:2; Rare:47 | ||||
| chr13:52012112-52012421 | Common:2; Rare:99; Clinvar:1 | ||||
| chr13:52159558-52159729 | Common:1; Rare:29 | ||||
| chr13:52455299-52455539 | Common:3; Rare:85 | ||||
| chr13:52652363-52652939 | Common:4; Rare:168 | ||||
| chr13:60163892-60164079 | Common:1; Rare:47 | ||||
| chr13:72727598-72727950 | Common:4; Rare:129 | ||||
| chr13:72781771-72782269 | Common:1; Rare:175 | ||||
| chr13:73058689-73059151 | Common:2; Rare:164 | ||||
| chr13:75549419-75549860 | Common:8; Rare:116 | ||||
| chr13:75635753-75635868 | Common:1; Rare:29 | ||||
| chr13:75636023-75636347 | Common:2; Rare:76 | ||||
| chr13:76992046-76992181 | Rare:63; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):2 |