| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47965821-47966076 | Common:2; Rare:45 | ||||
| chr3:47966092-47966215 | Common:1; Rare:21 | ||||
| chr3:48254264-48254278 | Rare:2 | ||||
| chr3:48427242-48427267 | Rare:3 | ||||
| chr3:48511581-48511886 | Common:1; Rare:38 | ||||
| chr3:48568498-48568820 | Common:2; Rare:80; Clinvar (pathogenic):1 | ||||
| chr3:48569375-48569662 | Rare:77; Clinvar:2 | ||||
| chr3:48569678-48569778 | Rare:28 | ||||
| chr3:48582481-48582932 | Rare:104; Clinvar (pathogenic):1 | ||||
| chr3:48593360-48593668 | Rare:91; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr3:48677910-48678045 | Rare:24 | ||||
| chr3:48741197-48741269 | Rare:16 | ||||
| chr3:49026374-49026544 | Common:1; Rare:48 | ||||
| chr3:49026585-49026837 | Common:2; Rare:72; Clinvar:1 | ||||
| chr3:49045189-49045318 | Rare:24 |