| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72781749-72782188 | Common:1; Rare:168 | ||||
| chr13:75537791-75538144 | Common:3; Rare:110 | ||||
| chr13:76991982-76992160 | Common:2; Rare:85; Clinvar:16; Clinvar (benign):9 | ||||
| chr13:77918704-77919075 | Common:2; Rare:84 | ||||
| chr13:77919397-77919599 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:78659121-78659253 | Common:2; Rare:89 | ||||
| chr13:79405720-79405875 | Common:1; Rare:51 | ||||
| chr13:79406227-79406314 | Common:1; Rare:27 | ||||
| chr13:80341310-80341478 | Rare:52 | ||||
| chr13:93226684-93226890 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr13:93226944-93227497 | Common:2; Rare:129; Clinvar:7; Clinvar (benign):2 | ||||
| chr13:94601600-94601954 | Common:3; Rare:112 | ||||
| chr13:95676937-95677274 | Common:4; Rare:117 | ||||
| chr13:96053313-96053602 | Common:2; Rare:126 | ||||
| chr13:97222152-97222531 | Rare:71 |