| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:70108419-70108586 | Rare:39 | ||||
| chr13:72727598-72727934 | Common:4; Rare:119 | ||||
| chr13:72781836-72782227 | Common:1; Rare:144 | ||||
| chr13:73058705-73059017 | Rare:99 | ||||
| chr13:74133773-74133848 | Common:2; Rare:12 | ||||
| chr13:75537777-75538109 | Common:3; Rare:107 | ||||
| chr13:75549401-75549837 | Common:8; Rare:118 | ||||
| chr13:76992050-76992181 | Rare:62; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr13:77027137-77027304 | Common:5; Rare:56 | ||||
| chr13:77697409-77697687 | Common:2; Rare:72 | ||||
| chr13:77918800-77918949 | Common:1; Rare:33 | ||||
| chr13:78659116-78659244 | Common:2; Rare:91 | ||||
| chr13:79405770-79405885 | Rare:44 | ||||
| chr13:95676894-95677218 | Common:3; Rare:118 | ||||
| chr13:96053315-96053435 | Rare:60 |