| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41439525-41439666 | Rare:42 | ||||
| chr19:41860107-41860285 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41860977-41861207 | Rare:74; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41884167-41884458 | Rare:78 | ||||
| chr19:41959282-41959441 | Common:1; Rare:55 | ||||
| chr19:42075805-42076209 | Rare:116 | ||||
| chr19:42217671-42217887 | Rare:82 | ||||
| chr19:42220112-42220386 | Common:2; Rare:70 | ||||
| chr19:42255071-42255384 | Common:1; Rare:110 | ||||
| chr19:42302316-42302570 | Rare:74 | ||||
| chr19:42423543-42423753 | Common:4; Rare:74 | ||||
| chr19:43504054-43504387 | Common:7; Rare:106 | ||||
| chr19:43575451-43575843 | Common:3; Rare:102 | ||||
| chr19:43580495-43580585 | Common:3; Rare:18 | ||||
| chr19:43595976-43596368 | Common:5; Rare:121 |