| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1103755-1104125 | Common:7; Rare:155 | ||||
| chr19:1105413-1105804 | Common:3; Rare:182; Clinvar (pathogenic):1 | ||||
| chr19:1132153-1132452 | Common:1; Rare:117 | ||||
| chr19:1354817-1355017 | Common:1; Rare:94 | ||||
| chr19:1905194-1905427 | Common:4; Rare:96 | ||||
| chr19:2328559-2328703 | Common:2; Rare:70 | ||||
| chr19:2475869-2476176 | Common:2; Rare:106 | ||||
| chr19:2841205-2841523 | Common:2; Rare:99 | ||||
| chr19:3061357-3061533 | Rare:52 | ||||
| chr19:3366475-3366634 | Common:3; Rare:43 | ||||
| chr19:3982805-3983221 | Common:5; Rare:146; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:4007481-4007763 | Common:3; Rare:105 | ||||
| chr19:4182499-4182710 | Common:1; Rare:80; Clinvar:1 | ||||
| chr19:4343443-4343580 | Rare:39 | ||||
| chr19:4518373-4518671 | Common:5; Rare:83 |