| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72781841-72782188 | Common:1; Rare:132 | ||||
| chr13:73058677-73059211 | Common:2; Rare:189 | ||||
| chr13:73060569-73060824 | Common:2; Rare:56 | ||||
| chr13:75549359-75549827 | Common:9; Rare:123 | ||||
| chr13:75760520-75760557 | Rare:8 | ||||
| chr13:75760615-75761011 | Common:3; Rare:126 | ||||
| chr13:75788748-75788955 | Common:1; Rare:28 | ||||
| chr13:76991956-76992188 | Common:3; Rare:111; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr13:77026860-77026969 | Common:2; Rare:35 | ||||
| chr13:77027130-77027312 | Common:6; Rare:63 | ||||
| chr13:78659121-78659235 | Common:2; Rare:83 | ||||
| chr13:79405695-79405909 | Common:1; Rare:64 | ||||
| chr13:79406210-79406339 | Common:3; Rare:40 | ||||
| chr13:79481003-79481521 | Common:2; Rare:198 | ||||
| chr13:80340009-80340297 | Common:1; Rare:55 |