| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77327048-77327172 | Rare:58 | ||||
| chr13:77697448-77697687 | Common:1; Rare:62 | ||||
| chr13:77918800-77919127 | Common:2; Rare:76 | ||||
| chr13:77919464-77919786 | Common:1; Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:78659057-78659236 | Common:2; Rare:125 | ||||
| chr13:79405409-79405459 | Common:1; Rare:8 | ||||
| chr13:79405722-79405898 | Common:1; Rare:57 | ||||
| chr13:79406210-79406359 | Common:3; Rare:47 | ||||
| chr13:79480992-79481488 | Common:2; Rare:190 | ||||
| chr13:79481868-79482002 | Rare:28 | ||||
| chr13:91398506-91398708 | Common:3; Rare:82 | ||||
| chr13:93227245-93227354 | Rare:19; Clinvar:2 | ||||
| chr13:94596129-94596329 | Common:2; Rare:70 | ||||
| chr13:94601596-94601930 | Common:3; Rare:99 | ||||
| chr13:95301376-95301613 | Rare:65 |