| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40056135-40056266 | Rare:16 | ||||
| chr19:40090878-40090990 | Common:1; Rare:30 | ||||
| chr19:40285243-40285537 | Common:1; Rare:108 | ||||
| chr19:40348377-40348751 | Common:4; Rare:123 | ||||
| chr19:40377814-40378187 | Common:2; Rare:134; Clinvar (benign):1 | ||||
| chr19:40413354-40413543 | Rare:54 | ||||
| chr19:40425990-40426148 | Common:1; Rare:46 | ||||
| chr19:40465687-40466084 | Common:3; Rare:123 | ||||
| chr19:40530408-40530541 | Common:1; Rare:40 | ||||
| chr19:40715074-40715148 | Rare:24 | ||||
| chr19:40716880-40717011 | Common:1; Rare:43 | ||||
| chr19:40750424-40750616 | Common:5; Rare:58 | ||||
| chr19:40798869-40799242 | Common:6; Rare:135 | ||||
| chr19:41262350-41262567 | Rare:41 | ||||
| chr19:41264569-41264823 | Common:1; Rare:83 |