| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75760546-75760966 | Common:4; Rare:231 | ||||
| chr13:76991934-76992210 | Common:7; Rare:231; Clinvar:39; Clinvar (benign):29; Clinvar (pathogenic):6 | ||||
| chr13:79405767-79406074 | Common:1; Rare:142 | ||||
| chr13:79406174-79406352 | Common:8; Rare:107 | ||||
| chr13:79481203-79481514 | Common:1; Rare:130 | ||||
| chr13:80341080-80341480 | Common:2; Rare:255 | ||||
| chr13:93226479-93227354 | Common:6; Rare:251; Clinvar:5; Clinvar (benign):3 | ||||
| chr13:94596110-94596354 | Common:3; Rare:155 | ||||
| chr13:95301346-95301603 | Common:1; Rare:116 | ||||
| chr13:95644519-95644843 | Common:2; Rare:145 | ||||
| chr13:95676819-95677247 | Common:9; Rare:291 | ||||
| chr13:96053321-96053602 | Common:4; Rare:234 | ||||
| chr13:97222138-97222485 | Rare:110 | ||||
| chr13:97433898-97434240 | Common:2; Rare:251 | ||||
| chr13:97976314-97976741 | Common:4; Rare:322 |