Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:60163816-60164063 | Common:2; Rare:57 | ||||
chr13:60396894-60397000 | Rare:31 | ||||
chr13:72727585-72727950 | Common:5; Rare:137 | ||||
chr13:72781828-72782227 | Common:1; Rare:149 | ||||
chr13:75549437-75549511 | Common:1; Rare:18 | ||||
chr13:75636004-75636382 | Common:2; Rare:91 | ||||
chr13:76992029-76992181 | Rare:69; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr13:77918768-77919132 | Common:2; Rare:84 | ||||
chr13:79405797-79405898 | Rare:33 | ||||
chr13:79406227-79406314 | Common:1; Rare:27 | ||||
chr13:94596133-94596335 | Common:2; Rare:67 | ||||
chr13:95301389-95301682 | Rare:77 | ||||
chr13:95676937-95677213 | Common:3; Rare:91 | ||||
chr13:96053353-96053615 | Common:3; Rare:104 | ||||
chr13:97222046-97222485 | Rare:76 |