| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10106522-10106642 | Common:1; Rare:55 | ||||
| chr19:10119812-10120058 | Common:1; Rare:98 | ||||
| chr19:10194327-10194481 | Common:1; Rare:46 | ||||
| chr19:10194585-10194731 | Common:1; Rare:33 | ||||
| chr19:10194861-10195225 | Common:2; Rare:151; Clinvar (benign):2 | ||||
| chr19:10231203-10231211 | |||||
| chr19:10231377-10231492 | Rare:22 | ||||
| chr19:10231500-10231587 | Rare:9 | ||||
| chr19:10251771-10252026 | Common:1; Rare:63 | ||||
| chr19:10252117-10252300 | Common:2; Rare:85 | ||||
| chr19:10252417-10252554 | Rare:50 | ||||
| chr19:10270534-10270604 | Rare:10 | ||||
| chr19:10270914-10271160 | Common:1; Rare:72 | ||||
| chr19:10283170-10283449 | Common:1; Rare:47 | ||||
| chr19:10286361-10286656 | Common:7; Rare:64 |