| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10928555-10928845 | Common:2; Rare:92 | ||||
| chr19:11339576-11339904 | Common:5; Rare:82 | ||||
| chr19:11374882-11375244 | Common:1; Rare:116 | ||||
| chr19:11381183-11381435 | Common:1; Rare:84; Clinvar:1 | ||||
| chr19:11383496-11383669 | Rare:46 | ||||
| chr19:11559201-11559465 | Common:4; Rare:79 | ||||
| chr19:11578704-11578883 | Rare:35 | ||||
| chr19:11578888-11579057 | Rare:36 | ||||
| chr19:11924961-11925112 | Common:6; Rare:40 | ||||
| chr19:12551430-12551718 | Common:2; Rare:81 | ||||
| chr19:12610740-12610994 | Rare:89 | ||||
| chr19:12647234-12647497 | Rare:98; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:12666674-12666866 | Rare:80; Clinvar:4 | ||||
| chr19:12696613-12696736 | Rare:58 | ||||
| chr19:12723925-12724192 | Common:1; Rare:50 |