| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35648060-35648429 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35648886-35648912 | Rare:7 | ||||
| chr19:35713117-35713563 | Common:3; Rare:109 | ||||
| chr19:35717432-35718061 | Common:4; Rare:166 | ||||
| chr19:35740445-35740965 | Common:6; Rare:188 | ||||
| chr19:35740971-35741278 | Common:4; Rare:108 | ||||
| chr19:35742390-35742637 | Common:2; Rare:77 | ||||
| chr19:35744635-35744728 | Rare:28 | ||||
| chr19:35744870-35745169 | Common:4; Rare:98 | ||||
| chr19:35745347-35745709 | Rare:109 | ||||
| chr19:35748221-35748680 | Common:3; Rare:127 | ||||
| chr19:35757660-35757675 | Rare:3 | ||||
| chr19:35757833-35758310 | Common:2; Rare:149 | ||||
| chr19:35758506-35758631 | Common:1; Rare:26 | ||||
| chr19:35775229-35775611 | Common:2; Rare:99 |