| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11361480-11361882 | Common:4; Rare:218 | ||||
| chr19:11374410-11375340 | Common:19; Rare:1411 | ||||
| chr19:11383115-11384574 | Common:4; Rare:965; Clinvar:8; Clinvar (benign):8 | ||||
| chr19:11419177-11419577 | Common:1; Rare:100 | ||||
| chr19:11434996-11435750 | Common:25; Rare:734; Clinvar:9; Clinvar (benign):14 | ||||
| chr19:11435970-11436410 | Common:2; Rare:188; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:11504960-11505583 | Common:8; Rare:684 | ||||
| chr19:11505566-11506160 | Common:7; Rare:603 | ||||
| chr19:11528650-11528990 | Common:1; Rare:95 | ||||
| chr19:11529015-11529415 | Common:6; Rare:275 | ||||
| chr19:11538456-11538856 | Common:10; Rare:185 | ||||
| chr19:11539875-11540411 | Common:5; Rare:226 | ||||
| chr19:11559081-11559606 | Common:22; Rare:632 | ||||
| chr19:11559610-11559800 | Rare:32 | ||||
| chr19:11577620-11578140 | Common:4; Rare:79 |