| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14125692-14125903 | Common:2; Rare:46 | ||||
| chr3:14945666-14945760 | Common:2; Rare:21 | ||||
| chr3:16301417-16301691 | Common:4; Rare:65 | ||||
| chr3:30608289-30608478 | Common:1; Rare:33 | ||||
| chr3:37302093-37302288 | Rare:51 | ||||
| chr3:37784795-37785074 | Common:1; Rare:66 | ||||
| chr3:39093633-39093906 | Common:2; Rare:42 | ||||
| chr3:40453171-40453421 | Common:5; Rare:53 | ||||
| chr3:41225331-41225762 | Rare:91; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:42632320-42632608 | Common:2; Rare:56 | ||||
| chr3:42654386-42654624 | Rare:70 | ||||
| chr3:44652526-44652568 | Rare:12 | ||||
| chr3:47867295-47867524 | Rare:45 | ||||
| chr3:48433879-48434103 | Common:1; Rare:38 | ||||
| chr3:49132123-49132375 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |