| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44164960-44165167 | Common:2; Rare:47 | ||||
| chr19:44212479-44212614 | Rare:47 | ||||
| chr19:44304992-44305163 | Rare:47 | ||||
| chr19:44356667-44356819 | Common:1; Rare:26 | ||||
| chr19:44643789-44643914 | Rare:42 | ||||
| chr19:44955241-44955401 | Common:2; Rare:45 | ||||
| chr19:45038954-45039097 | Rare:49 | ||||
| chr19:45079173-45079319 | Rare:38 | ||||
| chr19:45370544-45370727 | Common:1; Rare:56 | ||||
| chr19:45406339-45406694 | Common:3; Rare:90 | ||||
| chr19:45423839-45423949 | Common:2; Rare:30 | ||||
| chr19:45496949-45497283 | Common:3; Rare:99 | ||||
| chr19:45507228-45507516 | Common:1; Rare:74 | ||||
| chr19:45584774-45585023 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45730881-45731114 | Common:1; Rare:54 |