| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:32971893-32972298 | Common:4; Rare:116 | ||||
| chr19:33081081-33081245 | Common:2; Rare:62 | ||||
| chr19:33373522-33373821 | Common:2; Rare:103 | ||||
| chr19:33521750-33521931 | Rare:63; Clinvar:5 | ||||
| chr19:34172213-34172618 | Rare:143 | ||||
| chr19:34254526-34254602 | Rare:20 | ||||
| chr19:34359396-34359731 | Common:1; Rare:104 | ||||
| chr19:34396296-34396657 | Common:1; Rare:97; Clinvar (pathogenic):1 | ||||
| chr19:34404288-34404432 | Common:2; Rare:55 | ||||
| chr19:34428319-34428425 | Rare:45 | ||||
| chr19:34458511-34458924 | Common:2; Rare:77 | ||||
| chr19:34677045-34677370 | Common:7; Rare:54 | ||||
| chr19:34677482-34677803 | Common:7; Rare:94 | ||||
| chr19:34733813-34734280 | Common:3; Rare:132 | ||||
| chr19:34926823-34927106 | Common:1; Rare:84 |