| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:663147-663407 | Common:2; Rare:102 | ||||
| chr19:708790-709149 | Common:3; Rare:101 | ||||
| chr19:750989-751161 | Common:2; Rare:32 | ||||
| chr19:797124-797471 | Rare:147 | ||||
| chr19:804912-805158 | Common:1; Rare:109 | ||||
| chr19:859340-859696 | Common:2; Rare:105 | ||||
| chr19:893158-893484 | Common:3; Rare:139 | ||||
| chr19:913149-913274 | Rare:40 | ||||
| chr19:984260-984356 | Rare:33 | ||||
| chr19:1020813-1020853 | Rare:5 | ||||
| chr19:1021113-1021545 | Common:15; Rare:181 | ||||
| chr19:1026496-1026712 | Rare:81 | ||||
| chr19:1040005-1040163 | Common:1; Rare:50 | ||||
| chr19:1103794-1104115 | Common:4; Rare:135 | ||||
| chr19:1105385-1105777 | Common:3; Rare:183; Clinvar (pathogenic):1 |