| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48989737-48989953 | Rare:54 | ||||
| chr3:48990015-48990251 | Rare:48 | ||||
| chr3:48990368-48990508 | Rare:46 | ||||
| chr3:48990896-48991225 | Rare:52 | ||||
| chr3:49007155-49007438 | Common:2; Rare:119 | ||||
| chr3:49021503-49021772 | Rare:61; Clinvar:1 | ||||
| chr3:49022011-49022180 | Rare:59; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49028237-49028496 | Rare:75 | ||||
| chr3:49029264-49029564 | Common:2; Rare:186 | ||||
| chr3:49093475-49093670 | Rare:75 | ||||
| chr3:49093982-49094284 | Rare:72 | ||||
| chr3:49094297-49094443 | Common:1; Rare:36 | ||||
| chr3:49099367-49099600 | Rare:70; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr3:49104701-49104916 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49121830-49121954 | Common:2; Rare:43; Clinvar (benign):1 |