| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390974-39391442 | Common:1; Rare:181 | ||||
| chr19:39406695-39406880 | Rare:71 | ||||
| chr19:39480562-39480956 | Common:3; Rare:175; Clinvar (pathogenic):1 | ||||
| chr19:39846296-39846468 | Common:1; Rare:79 | ||||
| chr19:39970948-39971206 | Common:3; Rare:70 | ||||
| chr19:39996956-39997079 | Common:4; Rare:40 | ||||
| chr19:40056160-40056277 | Rare:18 | ||||
| chr19:40090858-40090990 | Common:1; Rare:38 | ||||
| chr19:40285197-40285568 | Common:1; Rare:129 | ||||
| chr19:40348388-40348739 | Common:4; Rare:117 | ||||
| chr19:40425970-40426147 | Common:1; Rare:56 | ||||
| chr19:40444261-40444466 | Common:3; Rare:66 | ||||
| chr19:40715068-40715171 | Rare:31 | ||||
| chr19:40750689-40750924 | Common:1; Rare:43 | ||||
| chr19:40751067-40751326 | Common:3; Rare:74 |