| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:65597806-65597955 | Common:2; Rare:49 | ||||
| chr3:67654567-67654674 | Rare:42 | ||||
| chr3:68005972-68006247 | Rare:37 | ||||
| chr3:69080351-69080444 | Rare:39 | ||||
| chr3:69542567-69542789 | Common:2; Rare:64 | ||||
| chr3:72848382-72848537 | Rare:53 | ||||
| chr3:73624218-73624486 | Common:5; Rare:87 | ||||
| chr3:79767940-79768093 | Rare:25 | ||||
| chr3:88058926-88059304 | Common:3; Rare:140 | ||||
| chr3:88149840-88150044 | Common:5; Rare:78 | ||||
| chr3:89107494-89107762 | Common:2; Rare:74 | ||||
| chr3:93979867-93980190 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062897-94063069 | Rare:44 | ||||
| chr3:96814442-96814652 | Rare:84 | ||||
| chr3:97764495-97764821 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 |