| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10928599-10928790 | Common:1; Rare:49 | ||||
| chr19:10960697-10961059 | Common:3; Rare:141 | ||||
| chr19:11089315-11089551 | Rare:50; Clinvar:12; Clinvar (pathogenic):1 | ||||
| chr19:11090334-11090621 | Common:2; Rare:88 | ||||
| chr19:11197494-11197633 | Common:1; Rare:36 | ||||
| chr19:11197757-11197974 | Common:2; Rare:66 | ||||
| chr19:11374929-11375245 | Common:1; Rare:84 | ||||
| chr19:11419287-11419450 | Rare:32 | ||||
| chr19:11435212-11435440 | Common:1; Rare:60 | ||||
| chr19:11559195-11559395 | Common:1; Rare:61 | ||||
| chr19:11578956-11579304 | Common:3; Rare:64 | ||||
| chr19:11738894-11739233 | Common:4; Rare:93 | ||||
| chr19:11766865-11767154 | Common:1; Rare:74 | ||||
| chr19:11924975-11925145 | Common:6; Rare:50 | ||||
| chr19:12365623-12365784 | Common:3; Rare:42 |