| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16197638-16198016 | Common:11; Rare:319 | ||||
| chr19:16324664-16324837 | Rare:61 | ||||
| chr19:16324742-16324934 | Rare:56 | ||||
| chr19:16471860-16472290 | Common:15; Rare:351 | ||||
| chr19:16496057-16496453 | Common:6; Rare:345; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:16542198-16542713 | Common:6; Rare:409 | ||||
| chr19:16571561-16571996 | Common:1; Rare:150 | ||||
| chr19:16572243-16572743 | Common:15; Rare:449 | ||||
| chr19:16628076-16628647 | Common:3; Rare:571 | ||||
| chr19:16628710-16629100 | Rare:152 | ||||
| chr19:16659660-16660040 | Common:6; Rare:245 | ||||
| chr19:16660044-16660440 | Common:9; Rare:412 | ||||
| chr19:16661011-16661207 | Common:2; Rare:120 | ||||
| chr19:16829251-16829501 | Common:4; Rare:135 | ||||
| chr19:17075378-17075850 | Common:18; Rare:560 |