| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54462569-54463350 | Common:9; Rare:432 | ||||
| chr19:54463578-54463847 | Common:3; Rare:129 | ||||
| chr19:54472812-54473480 | Common:4; Rare:151 | ||||
| chr19:55062852-55063763 | Common:22; Rare:511 | ||||
| chr19:55069349-55069639 | Common:2; Rare:123 | ||||
| chr19:55069750-55070016 | Common:3; Rare:66 | ||||
| chr19:55075665-55075992 | Common:6; Rare:131 | ||||
| chr19:55080430-55080969 | Common:3; Rare:258 | ||||
| chr19:55117527-55118006 | Common:21; Rare:308 | ||||
| chr19:55146280-55146650 | Common:4; Rare:195; Clinvar (benign):1 | ||||
| chr19:55146584-55147230 | Common:15; Rare:556; Clinvar:5; Clinvar (benign):19; Clinvar (pathogenic):2 | ||||
| chr19:55207237-55207366 | Common:1; Rare:45 | ||||
| chr19:55257915-55258667 | Common:15; Rare:412 | ||||
| chr19:55258906-55259570 | Common:11; Rare:479 | ||||
| chr19:55279982-55280191 | Common:1; Rare:77 |