Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45508606-45508682 | Common:1; Rare:14 | ||||
chr19:45509319-45509421 | Common:1; Rare:37 | ||||
chr19:45717228-45717540 | Common:1; Rare:95 | ||||
chr19:45767455-45767680 | Rare:69 | ||||
chr19:46133324-46133608 | Rare:49 | ||||
chr19:46404236-46404364 | Common:1; Rare:27 | ||||
chr19:46412098-46412381 | Common:1; Rare:104; Clinvar (pathogenic):1 | ||||
chr19:46412389-46412620 | Common:1; Rare:76 | ||||
chr19:46636167-46636259 | Common:1; Rare:10 | ||||
chr19:46659659-46659826 | Common:2; Rare:30 | ||||
chr19:46660264-46660340 | Rare:9 | ||||
chr19:46860778-46861133 | Common:3; Rare:114 | ||||
chr19:48966390-48966626 | Rare:73 | ||||
chr19:49150987-49151203 | Common:5; Rare:51 | ||||
chr19:49491486-49491797 | Common:1; Rare:101 |