| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40444617-40444966 | Common:2; Rare:112 | ||||
| chr19:40465699-40466008 | Common:2; Rare:100 | ||||
| chr19:40530261-40530550 | Common:3; Rare:82 | ||||
| chr19:40570524-40570780 | Common:2; Rare:80; Clinvar (pathogenic):1 | ||||
| chr19:40576653-40576930 | Common:4; Rare:78 | ||||
| chr19:40577072-40577158 | Common:1; Rare:28 | ||||
| chr19:40577384-40577426 | Rare:9 | ||||
| chr19:40598110-40598559 | Rare:94 | ||||
| chr19:40598628-40598738 | Rare:22 | ||||
| chr19:40600072-40600290 | Common:2; Rare:50; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr19:40601040-40601151 | Rare:25 | ||||
| chr19:40601204-40601498 | Rare:86; Clinvar:1 | ||||
| chr19:40605883-40606160 | Common:5; Rare:58 | ||||
| chr19:40613225-40613438 | Common:1; Rare:56; Clinvar (benign):2 | ||||
| chr19:40613747-40614045 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):2 |