| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584769-45585097 | Common:5; Rare:119; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692319-45692711 | Common:1; Rare:89 | ||||
| chr19:45730847-45731018 | Common:1; Rare:37 | ||||
| chr19:45769398-45769809 | Common:2; Rare:186 | ||||
| chr19:45772446-45772694 | Common:1; Rare:68; Clinvar:1 | ||||
| chr19:45782129-45782250 | Common:1; Rare:40 | ||||
| chr19:45782334-45782870 | Common:3; Rare:156 | ||||
| chr19:45902568-45902729 | Common:1; Rare:51 | ||||
| chr19:46382380-46382464 | Common:2; Rare:16 | ||||
| chr19:46383742-46383760 | Common:1; Rare:8 | ||||
| chr19:46600913-46601435 | Common:6; Rare:179; Clinvar (benign):3 | ||||
| chr19:46625048-46625169 | Common:1; Rare:24 | ||||
| chr19:46725877-46725919 | Rare:7 | ||||
| chr19:46745852-46746074 | Common:3; Rare:45 | ||||
| chr19:46746249-46746727 | Common:4; Rare:123 |