| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007201-49007434 | Common:2; Rare:92 | ||||
| chr3:49021503-49021731 | Rare:55; Clinvar:1 | ||||
| chr3:49132355-49132630 | Rare:94; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr3:49132840-49133141 | Rare:69; Clinvar:3 | ||||
| chr3:49340020-49340139 | Common:2; Rare:49 | ||||
| chr3:49358142-49358458 | Common:4; Rare:164 | ||||
| chr3:49411869-49412445 | Common:2; Rare:208 | ||||
| chr3:49429262-49429347 | Rare:22 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49689461-49689606 | Rare:46 | ||||
| chr3:49803177-49803299 | Rare:43 | ||||
| chr3:49856533-49856657 | Common:1; Rare:29 | ||||
| chr3:50267535-50267769 | Common:1; Rare:65 | ||||
| chr3:50273326-50273572 | Common:1; Rare:78 | ||||
| chr3:50299379-50299692 | Common:1; Rare:78 |