| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1269576-1269823 | Rare:113 | ||||
| chr19:1275309-1275598 | Common:1; Rare:148 | ||||
| chr19:1275731-1276148 | Common:2; Rare:189 | ||||
| chr19:1276666-1276801 | Rare:45 | ||||
| chr19:1354694-1355075 | Common:4; Rare:171 | ||||
| chr19:1383435-1383561 | Common:2; Rare:70 | ||||
| chr19:1383808-1383967 | Rare:57; Clinvar (benign):2 | ||||
| chr19:1401437-1401682 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):6 | ||||
| chr19:1407121-1407611 | Common:3; Rare:193 | ||||
| chr19:1407660-1407859 | Rare:43 | ||||
| chr19:1438255-1438477 | Rare:91 | ||||
| chr19:1479102-1479365 | Common:1; Rare:100 | ||||
| chr19:1479480-1479667 | Common:1; Rare:46 | ||||
| chr19:1490275-1490510 | Common:4; Rare:84 | ||||
| chr19:1512987-1513236 | Common:1; Rare:87 |