| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79069005-79069282 | Common:8; Rare:122 | ||||
| chr18:79679359-79679551 | Common:1; Rare:91 | ||||
| chr19:633506-633763 | Common:8; Rare:118 | ||||
| chr19:663126-663436 | Common:3; Rare:125 | ||||
| chr19:893158-893495 | Common:3; Rare:150 | ||||
| chr19:913155-913274 | Rare:38 | ||||
| chr19:984277-984348 | Rare:22 | ||||
| chr19:1103794-1104104 | Common:4; Rare:131 | ||||
| chr19:1132130-1132374 | Common:1; Rare:113 | ||||
| chr19:1354786-1354999 | Common:2; Rare:89 | ||||
| chr19:1605400-1605649 | Common:3; Rare:95 | ||||
| chr19:2328550-2328703 | Common:2; Rare:74 | ||||
| chr19:2944908-2945181 | Common:5; Rare:94 | ||||
| chr19:3366463-3366623 | Common:3; Rare:36 | ||||
| chr19:3982797-3983292 | Common:5; Rare:179; Clinvar:1; Clinvar (benign):6 |