| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53867679-53867953 | Common:1; Rare:70 | ||||
| chr19:53869454-53869778 | Common:2; Rare:88 | ||||
| chr19:54102581-54102916 | Common:6; Rare:94 | ||||
| chr19:54114491-54114769 | Rare:92 | ||||
| chr19:54115225-54115470 | Common:2; Rare:73; Clinvar (benign):2 | ||||
| chr19:54115603-54115827 | Common:3; Rare:62; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:54137516-54137951 | Common:3; Rare:136 | ||||
| chr19:54159389-54159578 | Common:1; Rare:77 | ||||
| chr19:54159640-54160199 | Common:1; Rare:182 | ||||
| chr19:54189306-54189649 | Common:3; Rare:109 | ||||
| chr19:54189654-54189731 | Common:2; Rare:24 | ||||
| chr19:54190087-54190404 | Common:3; Rare:97; Clinvar:1 | ||||
| chr19:54190424-54190723 | Common:5; Rare:85; Clinvar (benign):1 | ||||
| chr19:54190938-54191442 | Common:7; Rare:184; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:54200640-54200935 | Common:5; Rare:104 |