| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:752686-752840 | Rare:40 | ||||
| chr19:782559-782877 | Common:2; Rare:184 | ||||
| chr19:783082-783482 | Common:2; Rare:148 | ||||
| chr19:800576-800755 | Rare:124 | ||||
| chr19:823610-824040 | Common:5; Rare:205 | ||||
| chr19:860505-860714 | Rare:136; Clinvar (pathogenic):2 | ||||
| chr19:926580-927323 | Common:2; Rare:364 | ||||
| chr19:934860-935260 | Common:7; Rare:236 | ||||
| chr19:953170-953520 | Common:12; Rare:189 | ||||
| chr19:958978-959203 | Common:2; Rare:91 | ||||
| chr19:982407-982950 | Common:16; Rare:221 | ||||
| chr19:1028149-1028287 | Rare:15 | ||||
| chr19:1028650-1028844 | Rare:42 | ||||
| chr19:1074740-1075107 | Common:34; Rare:391 | ||||
| chr19:1161770-1162040 | Common:3; Rare:80 |