| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:32691659-32691784 | Rare:34 | ||||
| chr19:32971921-32972284 | Common:4; Rare:104 | ||||
| chr19:33081037-33081233 | Common:4; Rare:66 | ||||
| chr19:33373545-33373821 | Common:2; Rare:92 | ||||
| chr19:33521762-33521947 | Rare:56; Clinvar:4 | ||||
| chr19:34172396-34172684 | Common:1; Rare:107 | ||||
| chr19:34254484-34254603 | Rare:37 | ||||
| chr19:34364922-34365338 | Common:1; Rare:160; Clinvar (pathogenic):1 | ||||
| chr19:34396367-34396657 | Common:1; Rare:80 | ||||
| chr19:34428319-34428441 | Rare:52 | ||||
| chr19:34677230-34677819 | Common:8; Rare:156 | ||||
| chr19:34733790-34734291 | Common:3; Rare:140 | ||||
| chr19:34926823-34927061 | Common:1; Rare:77 | ||||
| chr19:35138586-35139090 | Common:1; Rare:111 | ||||
| chr19:35139092-35139176 | Common:1; Rare:26 |