| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:18423667-18423835 | Common:1; Rare:34 | ||||
| chr3:26622054-26622158 | Rare:21 | ||||
| chr3:39384297-39384435 | Common:3; Rare:22 | ||||
| chr3:40453165-40453422 | Common:6; Rare:56 | ||||
| chr3:44685615-44685671 | Rare:19 | ||||
| chr3:55423831-55424086 | Common:2; Rare:44 | ||||
| chr3:61743136-61743272 | Common:2; Rare:28 | ||||
| chr3:72738815-72738941 | Common:3; Rare:48 | ||||
| chr3:75435099-75435379 | Common:2; Rare:94 | ||||
| chr3:75641103-75641304 | Rare:37 | ||||
| chr3:77043052-77043099 | Rare:5 | ||||
| chr3:80770335-80770625 | Common:3; Rare:50 | ||||
| chr3:81761462-81761567 | Common:4; Rare:37; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:85780792-85780914 | Rare:24 | ||||
| chr3:87089203-87089343 | Common:1; Rare:30 |