| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021490-49021710 | Rare:55; Clinvar:1 | ||||
| chr3:49022006-49022164 | Rare:51; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029270-49029470 | Common:1; Rare:115 | ||||
| chr3:49099581-49099762 | Rare:62; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:49100030-49100232 | Rare:62; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:49104687-49104914 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:49132831-49133150 | Rare:74; Clinvar:3 | ||||
| chr3:49166284-49166442 | Common:1; Rare:42 | ||||
| chr3:49339975-49340122 | Common:2; Rare:72 | ||||
| chr3:49358061-49358134 | Rare:37 | ||||
| chr3:49411820-49412213 | Common:1; Rare:125 | ||||
| chr3:49429262-49429330 | Rare:18 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49689447-49689613 | Rare:55 | ||||
| chr3:49803050-49803389 | Common:3; Rare:105 |