| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:70108411-70108586 | Rare:40 | ||||
| chr13:72727544-72727978 | Common:7; Rare:175 | ||||
| chr13:72781737-72782285 | Common:1; Rare:194 | ||||
| chr13:74133761-74133936 | Common:3; Rare:43 | ||||
| chr13:74134004-74134047 | Rare:14 | ||||
| chr13:74134258-74134554 | Common:3; Rare:110 | ||||
| chr13:75537768-75538114 | Common:3; Rare:112 | ||||
| chr13:75549359-75549834 | Common:9; Rare:127 | ||||
| chr13:76992034-76992215 | Common:1; Rare:82; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr13:77027137-77027274 | Common:5; Rare:45 | ||||
| chr13:77327074-77327305 | Common:1; Rare:86 | ||||
| chr13:77918692-77918949 | Common:2; Rare:56 | ||||
| chr13:77919397-77919599 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:78659059-78659241 | Common:2; Rare:125 | ||||
| chr13:79405779-79405909 | Rare:44 |