| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:14440923-14441133 | Common:3; Rare:66 | ||||
| chr5:14664569-14664664 | Common:2; Rare:41 | ||||
| chr5:16465694-16465902 | Rare:42 | ||||
| chr5:16508820-16509067 | Common:1; Rare:44 | ||||
| chr5:31532052-31532356 | Common:3; Rare:87 | ||||
| chr5:31854720-31855000 | Common:1; Rare:93 | ||||
| chr5:32174277-32174402 | Common:1; Rare:45 | ||||
| chr5:32444654-32444848 | Rare:84 | ||||
| chr5:32585352-32585624 | Common:2; Rare:99 | ||||
| chr5:33440617-33441109 | Common:7; Rare:137 | ||||
| chr5:34008017-34008222 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656159-34656473 | Common:3; Rare:79 | ||||
| chr5:34839045-34839203 | Rare:57 | ||||
| chr5:34839264-34839398 | Common:2; Rare:40 | ||||
| chr5:34915218-34915294 | Rare:20 |