| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45370493-45370782 | Common:2; Rare:95; Clinvar:1 | ||||
| chr19:45406321-45406709 | Common:3; Rare:94 | ||||
| chr19:45423323-45423648 | Common:2; Rare:77; Clinvar (benign):2 | ||||
| chr19:45423838-45424022 | Common:2; Rare:41 | ||||
| chr19:45424373-45424602 | Rare:33 | ||||
| chr19:45496959-45497293 | Common:3; Rare:100 | ||||
| chr19:45506436-45506625 | Common:2; Rare:41 | ||||
| chr19:45506792-45507022 | Common:1; Rare:73 | ||||
| chr19:45584760-45585183 | Common:5; Rare:142; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692299-45692722 | Common:1; Rare:102 | ||||
| chr19:45730857-45731103 | Common:1; Rare:56 | ||||
| chr19:46346948-46347182 | Common:3; Rare:84 | ||||
| chr19:46382386-46382426 | Rare:6 | ||||
| chr19:46600913-46601432 | Common:6; Rare:178; Clinvar (benign):3 | ||||
| chr19:46608203-46608585 | Common:1; Rare:76; Clinvar (benign):7 |