| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49664359-49664766 | Common:2; Rare:144 | ||||
| chr19:49665370-49666076 | Common:12; Rare:501; Clinvar (pathogenic):2 | ||||
| chr19:49683700-49684316 | Common:12; Rare:358 | ||||
| chr19:49766375-49767250 | Common:8; Rare:674 | ||||
| chr19:49851015-49851265 | Common:2; Rare:186 | ||||
| chr19:49867481-49867689 | Common:6; Rare:101; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:49876052-49876452 | Rare:154 | ||||
| chr19:49877163-49877742 | Common:6; Rare:282 | ||||
| chr19:49877836-49878221 | Common:7; Rare:221 | ||||
| chr19:49928846-49929242 | Common:7; Rare:189 | ||||
| chr19:49929404-49929627 | Common:8; Rare:146 | ||||
| chr19:49958115-49958278 | Common:2; Rare:85 | ||||
| chr19:50025360-50026020 | Common:15; Rare:296 | ||||
| chr19:50329478-50329674 | Common:1; Rare:41 | ||||
| chr19:50333460-50334020 | Common:6; Rare:173 |