| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41439499-41439735 | Common:2; Rare:69 | ||||
| chr19:41439846-41440075 | Common:3; Rare:98 | ||||
| chr19:41755363-41755578 | Rare:38 | ||||
| chr19:41859512-41859957 | Common:1; Rare:123; Clinvar:1 | ||||
| chr19:41860070-41860333 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41860733-41860841 | Rare:45; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr19:41883129-41883259 | Common:1; Rare:25 | ||||
| chr19:41883284-41883482 | Rare:41 | ||||
| chr19:41884095-41884512 | Rare:111 | ||||
| chr19:41904464-41904836 | Common:2; Rare:65 | ||||
| chr19:41957864-41958044 | Rare:40 | ||||
| chr19:41958543-41958788 | Common:3; Rare:81 | ||||
| chr19:41959244-41959481 | Common:1; Rare:80 | ||||
| chr19:42074934-42075238 | Common:1; Rare:61 | ||||
| chr19:42075720-42076307 | Common:5; Rare:168 |