| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58326849-58327051 | Common:1; Rare:47 | ||||
| chr19:58347610-58347779 | Common:8; Rare:80 | ||||
| chr19:58408449-58408679 | Common:2; Rare:73 | ||||
| chr19:58499216-58499581 | Common:2; Rare:122; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:58558320-58558731 | Rare:134 | ||||
| chr19:58558931-58559132 | Common:1; Rare:61 | ||||
| chr2:264561-264984 | Common:4; Rare:161 | ||||
| chr2:3377790-3377937 | Rare:40 | ||||
| chr2:3519510-3519727 | Common:2; Rare:54 | ||||
| chr2:3558225-3558559 | Common:6; Rare:133 | ||||
| chr2:3574997-3575354 | Common:3; Rare:98; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423163-9423289 | Common:1; Rare:27 | ||||
| chr2:9423471-9423700 | Rare:72 | ||||
| chr2:9555631-9556019 | Common:2; Rare:128 | ||||
| chr2:10302713-10302993 | Common:5; Rare:85 |