| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44212441-44212581 | Rare:37 | ||||
| chr19:44356635-44356851 | Common:1; Rare:48 | ||||
| chr19:44500505-44500636 | Common:1; Rare:37 | ||||
| chr19:44643793-44643918 | Rare:39 | ||||
| chr19:44955198-44955427 | Common:4; Rare:68 | ||||
| chr19:45038965-45039108 | Rare:51 | ||||
| chr19:45079165-45079321 | Rare:41 | ||||
| chr19:45092820-45092953 | Common:1; Rare:40 | ||||
| chr19:45370549-45370731 | Common:2; Rare:53 | ||||
| chr19:45406331-45406703 | Common:3; Rare:92 | ||||
| chr19:45423488-45423797 | Common:3; Rare:64; Clinvar (benign):1 | ||||
| chr19:45423839-45423993 | Common:2; Rare:34 | ||||
| chr19:45424325-45424608 | Common:4; Rare:41 | ||||
| chr19:45450738-45450993 | Common:4; Rare:47 | ||||
| chr19:45507225-45507511 | Common:1; Rare:73 |