| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51975033-51975132 | Common:1; Rare:37 | ||||
| chr3:51983398-51983578 | Common:1; Rare:39 | ||||
| chr3:51995827-51996051 | Common:3; Rare:82 | ||||
| chr3:52154364-52154521 | Common:1; Rare:43 | ||||
| chr3:52154675-52154735 | Rare:9 | ||||
| chr3:52239044-52239275 | Common:2; Rare:80 | ||||
| chr3:52278315-52278440 | Rare:51 | ||||
| chr3:52278582-52278791 | Rare:76 | ||||
| chr3:52287727-52287863 | Common:2; Rare:52 | ||||
| chr3:52288005-52288111 | Rare:38 | ||||
| chr3:52409877-52410219 | Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:52410335-52410582 | Rare:47 | ||||
| chr3:52455425-52455638 | Common:2; Rare:70 | ||||
| chr3:52527329-52527668 | Common:3; Rare:96 | ||||
| chr3:52528446-52528901 | Common:3; Rare:145 |