| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:984225-984348 | Common:1; Rare:46 | ||||
| chr19:1103737-1104119 | Common:8; Rare:159 | ||||
| chr19:1105203-1105804 | Common:4; Rare:271; Clinvar (pathogenic):1 | ||||
| chr19:1132100-1132487 | Common:2; Rare:152 | ||||
| chr19:1155124-1155320 | Rare:58 | ||||
| chr19:1174247-1174365 | Common:1; Rare:50 | ||||
| chr19:1248457-1248588 | Common:1; Rare:44 | ||||
| chr19:1269057-1269360 | Common:2; Rare:115 | ||||
| chr19:1354786-1355033 | Common:3; Rare:119 | ||||
| chr19:1513008-1513304 | Common:1; Rare:108 | ||||
| chr19:1592642-1592983 | Common:2; Rare:177 | ||||
| chr19:2096090-2096388 | Rare:96 | ||||
| chr19:2282138-2282385 | Common:3; Rare:71 | ||||
| chr19:2328565-2328703 | Common:2; Rare:70 | ||||
| chr19:2841205-2841533 | Common:2; Rare:102 |