| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45469729-45469938 | Common:3; Rare:62 | ||||
| chr19:45478638-45478698 | Rare:37 | ||||
| chr19:45478710-45478909 | Common:1; Rare:79 | ||||
| chr19:45479030-45479134 | Common:1; Rare:28 | ||||
| chr19:45496924-45497337 | Common:3; Rare:117 | ||||
| chr19:45506556-45506689 | Common:1; Rare:43 | ||||
| chr19:45506814-45506863 | Common:1; Rare:16 | ||||
| chr19:45507227-45507534 | Common:1; Rare:83 | ||||
| chr19:45584199-45584711 | Common:3; Rare:146; Clinvar:2 | ||||
| chr19:45584717-45585012 | Common:4; Rare:117; Clinvar:3; Clinvar (benign):4 | ||||
| chr19:45615980-45616360 | Common:1; Rare:90 | ||||
| chr19:45632553-45632588 | Rare:5 | ||||
| chr19:45639345-45639488 | Common:1; Rare:44 | ||||
| chr19:45642193-45642660 | Common:2; Rare:128 | ||||
| chr19:45646035-45646243 | Rare:35 |