| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46979920-46980320 | Common:3; Rare:83; Clinvar:1 | ||||
| chr3:47162879-47163843 | Common:8; Rare:424 | ||||
| chr3:47163820-47164573 | Common:10; Rare:901; Clinvar (pathogenic):3 | ||||
| chr3:47281486-47281886 | Common:1; Rare:108 | ||||
| chr3:47281892-47282292 | Common:2; Rare:90 | ||||
| chr3:47282330-47283939 | Common:8; Rare:970 | ||||
| chr3:47380452-47381165 | Common:6; Rare:952 | ||||
| chr3:47381373-47381750 | Rare:214 | ||||
| chr3:47474962-47475362 | Common:2; Rare:108 | ||||
| chr3:47475709-47476177 | Common:24; Rare:746 | ||||
| chr3:47511400-47512457 | Common:7; Rare:276 | ||||
| chr3:47512878-47513286 | Common:3; Rare:123 | ||||
| chr3:47513289-47513603 | Common:7; Rare:654 | ||||
| chr3:47513566-47514000 | Common:9; Rare:428 | ||||
| chr3:47578128-47578528 | Rare:181 |