| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37506728-37506953 | Rare:46 | ||||
| chr19:37507030-37507208 | Common:2; Rare:50 | ||||
| chr19:37551268-37551420 | Rare:49 | ||||
| chr19:37594753-37594892 | Rare:37 | ||||
| chr19:37655424-37655469 | Rare:23 | ||||
| chr19:37719721-37719791 | Rare:24 | ||||
| chr19:37779566-37779651 | Rare:22 | ||||
| chr19:37817275-37817473 | Common:1; Rare:38 | ||||
| chr19:38315763-38316080 | Rare:111 | ||||
| chr19:38336315-38336459 | Common:1; Rare:32 | ||||
| chr19:38374407-38374836 | Rare:165 | ||||
| chr19:38618956-38619252 | Common:3; Rare:87 | ||||
| chr19:38647372-38647737 | Common:3; Rare:129 | ||||
| chr19:38899572-38900018 | Rare:132 | ||||
| chr19:38930742-38930987 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 |