| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40425990-40426109 | Rare:35 | ||||
| chr19:40623535-40623608 | Rare:25 | ||||
| chr19:40716872-40716984 | Common:1; Rare:30 | ||||
| chr19:40750426-40750913 | Common:6; Rare:120 | ||||
| chr19:40751080-40751433 | Common:3; Rare:112 | ||||
| chr19:40777934-40778280 | Common:1; Rare:97 | ||||
| chr19:41193094-41193290 | Common:1; Rare:64 | ||||
| chr19:41219045-41219227 | Rare:31 | ||||
| chr19:41262371-41262571 | Rare:35 | ||||
| chr19:41264944-41265109 | Common:2; Rare:36 | ||||
| chr19:41397332-41397853 | Common:11; Rare:160; Clinvar (benign):5 | ||||
| chr19:41860157-41860285 | Rare:49; Clinvar:2 | ||||
| chr19:42075766-42076199 | Common:5; Rare:127 | ||||
| chr19:42220120-42220358 | Common:2; Rare:64 | ||||
| chr19:42302306-42302414 | Rare:37 |