| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476867-50476940 | Rare:21 | ||||
| chr19:50511099-50511610 | Common:5; Rare:170 | ||||
| chr19:50723181-50723387 | Common:2; Rare:49 | ||||
| chr19:50804576-50804944 | Common:7; Rare:107 | ||||
| chr19:50870577-50870675 | Common:2; Rare:26 | ||||
| chr19:51019707-51019881 | Common:4; Rare:33 | ||||
| chr19:51027637-51027761 | Rare:16 | ||||
| chr19:51064902-51065036 | Common:1; Rare:40 | ||||
| chr19:51224951-51225120 | Rare:42 | ||||
| chr19:51250911-51251160 | Common:3; Rare:62 | ||||
| chr19:51339709-51340013 | Common:1; Rare:61 | ||||
| chr19:51366283-51366551 | Common:5; Rare:82; Clinvar (benign):2 | ||||
| chr19:51390468-51390644 | Common:1; Rare:58 | ||||
| chr19:51571193-51571304 | Common:4; Rare:32 | ||||
| chr19:51645535-51645783 | Common:10; Rare:41 |