| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38930290-38930660 | Common:3; Rare:233; Clinvar:3; Clinvar (benign):4 | ||||
| chr19:38930635-38931088 | Common:11; Rare:356; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr19:38975630-38975960 | Common:3; Rare:163 | ||||
| chr19:39031268-39031567 | Common:3; Rare:128 | ||||
| chr19:39031530-39032089 | Common:12; Rare:332 | ||||
| chr19:39032455-39032589 | Common:1; Rare:28 | ||||
| chr19:39032501-39032706 | Common:2; Rare:42 | ||||
| chr19:39083880-39084620 | Common:14; Rare:396 | ||||
| chr19:39125509-39125883 | Common:4; Rare:257 | ||||
| chr19:39156401-39156780 | Common:9; Rare:182 | ||||
| chr19:39341820-39342329 | Common:2; Rare:270 | ||||
| chr19:39342373-39342532 | Common:6; Rare:144 | ||||
| chr19:39390550-39390800 | Rare:75 | ||||
| chr19:39390789-39391511 | Common:3; Rare:742; Clinvar:3 | ||||
| chr19:39406516-39407052 | Common:2; Rare:347 |