| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:9545977-9546372 | Common:10; Rare:97 | ||||
| chr5:10249866-10250183 | Common:16; Rare:146 | ||||
| chr5:10250187-10250427 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353590-10353896 | Common:3; Rare:113 | ||||
| chr5:16465717-16465913 | Rare:39 | ||||
| chr5:31532043-31532352 | Common:3; Rare:87 | ||||
| chr5:32174254-32174462 | Common:4; Rare:76 | ||||
| chr5:32444667-32444988 | Common:1; Rare:107 | ||||
| chr5:32711102-32711322 | Rare:33 | ||||
| chr5:33440597-33441134 | Common:7; Rare:149 | ||||
| chr5:33891943-33892289 | Rare:81 | ||||
| chr5:34008027-34008251 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656150-34656473 | Common:3; Rare:82 | ||||
| chr5:34915212-34915374 | Rare:45 | ||||
| chr5:35856766-35856926 | Rare:24 |