| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:74110949-74111247 | Common:3; Rare:45 | ||||
| chr10:74314674-74314873 | Rare:42; Clinvar:2 | ||||
| chr10:74543226-74543523 | Common:2; Rare:39 | ||||
| chr10:74711254-74711388 | Rare:29 | ||||
| chr10:74715416-74715525 | Rare:10 | ||||
| chr10:74722202-74722271 | Rare:13 | ||||
| chr10:75194751-75194851 | Rare:19 | ||||
| chr10:75409585-75409724 | Common:2; Rare:38 | ||||
| chr10:77771376-77771379 | |||||
| chr10:77940694-77940835 | Rare:19 | ||||
| chr10:78036888-78037191 | Common:6; Rare:69; Clinvar:1 | ||||
| chr10:78040203-78040591 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr10:79279842-79279980 | Rare:31 | ||||
| chr10:79513437-79513739 | Common:3; Rare:49 | ||||
| chr10:79699031-79699111 | Common:1; Rare:21 |