| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:633446-633745 | Common:8; Rare:138 | ||||
| chr19:663066-663445 | Common:3; Rare:142 | ||||
| chr19:676120-676397 | Common:4; Rare:81 | ||||
| chr19:893135-893495 | Common:3; Rare:159 | ||||
| chr19:913128-913289 | Rare:48 | ||||
| chr19:984274-984348 | Rare:22 | ||||
| chr19:1021238-1021522 | Common:11; Rare:120 | ||||
| chr19:1103773-1104104 | Common:6; Rare:141 | ||||
| chr19:1105164-1105804 | Common:4; Rare:284; Clinvar (pathogenic):1 | ||||
| chr19:1132164-1132444 | Common:1; Rare:110 | ||||
| chr19:1174289-1174599 | Common:2; Rare:91 | ||||
| chr19:1244022-1244161 | Common:1; Rare:61 | ||||
| chr19:1248275-1248608 | Common:2; Rare:106 | ||||
| chr19:1251685-1251892 | Common:1; Rare:89 | ||||
| chr19:1354817-1355002 | Rare:77 |