| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77027137-77027301 | Common:5; Rare:54 | ||||
| chr13:77740865-77741187 | Common:1; Rare:65 | ||||
| chr13:77918653-77919139 | Common:3; Rare:111 | ||||
| chr13:77919160-77919197 | Rare:14 | ||||
| chr13:77919361-77919854 | Common:1; Rare:150; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:78659121-78659253 | Common:2; Rare:89 | ||||
| chr13:79405763-79405898 | Common:1; Rare:48 | ||||
| chr13:79406217-79406341 | Common:3; Rare:40 | ||||
| chr13:79481009-79481479 | Common:2; Rare:183 | ||||
| chr13:80338840-80339241 | Common:1; Rare:81 | ||||
| chr13:80339290-80339350 | Common:1; Rare:10 | ||||
| chr13:93226590-93226891 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr13:94478945-94479829 | Common:2; Rare:235 | ||||
| chr13:94479946-94480233 | Rare:49 | ||||
| chr13:94596106-94596308 | Common:1; Rare:79 |