| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38975718-38975844 | Common:1; Rare:26 | ||||
| chr19:39084105-39084371 | Rare:70 | ||||
| chr19:39390861-39391431 | Common:1; Rare:215 | ||||
| chr19:39406710-39406852 | Rare:55 | ||||
| chr19:39435850-39436167 | Common:7; Rare:116 | ||||
| chr19:39480608-39480925 | Common:3; Rare:157; Clinvar (pathogenic):1 | ||||
| chr19:39846307-39846539 | Common:1; Rare:112 | ||||
| chr19:39970923-39971215 | Common:4; Rare:82 | ||||
| chr19:39996925-39997118 | Common:5; Rare:62 | ||||
| chr19:40056167-40056266 | Rare:15 | ||||
| chr19:40090899-40090958 | Rare:17 | ||||
| chr19:40285243-40285623 | Common:3; Rare:131 | ||||
| chr19:40348364-40348739 | Common:4; Rare:123 | ||||
| chr19:40425989-40426147 | Common:1; Rare:46 | ||||
| chr19:40715076-40715215 | Rare:36 |